Canonical Allele Identifier: CA2422497690

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.31627437_31627438delinsCA , CM000685.2:g.31627437_31627438delinsCA	GRCh38
NC_000023.10:g.31645554_31645555delinsCA , CM000685.1:g.31645554_31645555delinsCA	GRCh37
NC_000023.9:g.31555475_31555476delinsCA	NCBI36
NG_012232.1:g.1717172_1717173delinsTG , LRG_199:g.1717172_1717173delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.3063+235_3063+236delinsTG	ENSP00000350765.3:n.3063+235_3063+236delinsTG
ENST00000682238.1:c.837+235_837+236delinsTG	ENSP00000508124.1:n.837+235_837+236delinsTG
ENST00000683450.1:n.1682+235_1682+236delinsTG
ENST00000683851.1:n.2113_2114delinsTG
ENST00000683957.1:n.1709+235_1709+236delinsTG
ENST00000684130.1:c.837+235_837+236delinsTG	ENSP00000508037.1:n.837+235_837+236delinsTG
ENST00000357033.9:c.8217+235_8217+236delinsTG MANE Select	ENSP00000354923.3:n.8217+235_8217+236delinsTG
ENST00000619831.5:c.4185+235_4185+236delinsTG	ENSP00000479270.2:n.4185+235_4185+236delinsTG
ENST00000620040.5:c.837+235_837+236delinsTG	ENSP00000478150.2:n.837+235_837+236delinsTG
ENST00000680961.1:c.837+235_837+236delinsTG	ENSP00000506386.1:n.837+235_837+236delinsTG
ENST00000681646.1:n.1878+235_1878+236delinsTG
ENST00000357033.8:c.8217+235_8217+236delinsTG	ENSP00000354923.3:n.8217+235_8217+236delinsTG
ENST00000358062.6:c.1305+235_1305+236delinsTG	ENSP00000350765.2:n.1305+235_1305+236delinsTG
ENST00000359836.5:c.837+235_837+236delinsTG	ENSP00000352894.1:n.837+235_837+236delinsTG
ENST00000378677.6:c.8205+235_8205+236delinsTG	ENSP00000367948.2:n.8205+235_8205+236delinsTG
ENST00000378707.7:c.837+235_837+236delinsTG	ENSP00000367979.3:n.837+235_837+236delinsTG
ENST00000474231.5:c.837+235_837+236delinsTG	ENSP00000417123.1:n.837+235_837+236delinsTG
ENST00000541735.5:c.837+235_837+236delinsTG	ENSP00000444119.1:n.837+235_837+236delinsTG
ENST00000619831.4:c.8202+235_8202+236delinsTG	ENSP00000479270.1:n.8202+235_8202+236delinsTG
ENST00000620040.4:c.8214+235_8214+236delinsTG	ENSP00000478150.1:n.8214+235_8214+236delinsTG
NM_000109.3:c.8193+235_8193+236delinsTG	NP_000100.2:n.8193+235_8193+236delinsTG
NM_004006.2:c.8217+235_8217+236delinsTG , LRG_199t1:c.8217+235_8217+236delinsTG	NP_003997.1:n.8217+235_8217+236delinsTG
NM_004009.3:c.8205+235_8205+236delinsTG	NP_004000.1:n.8205+235_8205+236delinsTG
NM_004010.3:c.7848+235_7848+236delinsTG	NP_004001.1:n.7848+235_7848+236delinsTG
NM_004011.3:c.4194+235_4194+236delinsTG	NP_004002.2:n.4194+235_4194+236delinsTG
NM_004012.3:c.4185+235_4185+236delinsTG	NP_004003.1:n.4185+235_4185+236delinsTG
NM_004013.2:c.837+235_837+236delinsTG	NP_004004.1:n.837+235_837+236delinsTG
NM_004020.3:c.837+235_837+236delinsTG	NP_004011.2:n.837+235_837+236delinsTG
NM_004021.2:c.837+235_837+236delinsTG	NP_004012.1:n.837+235_837+236delinsTG
NM_004022.2:c.837+235_837+236delinsTG	NP_004013.1:n.837+235_837+236delinsTG
NM_004023.2:c.837+235_837+236delinsTG	NP_004014.1:n.837+235_837+236delinsTG
XM_006724468.2:c.8217+235_8217+236delinsTG	XP_006724531.1:n.8217+235_8217+236delinsTG
XM_006724469.2:c.8193+235_8193+236delinsTG	XP_006724532.1:n.8193+235_8193+236delinsTG
XM_006724470.2:c.8217+235_8217+236delinsTG	XP_006724533.1:n.8217+235_8217+236delinsTG
XM_006724471.2:c.8217+235_8217+236delinsTG	XP_006724534.1:n.8217+235_8217+236delinsTG
XM_006724472.2:c.8088+235_8088+236delinsTG	XP_006724535.1:n.8088+235_8088+236delinsTG
XM_006724473.2:c.8079+235_8079+236delinsTG	XP_006724536.1:n.8079+235_8079+236delinsTG
XM_006724474.2:c.8217+235_8217+236delinsTG	XP_006724537.1:n.8217+235_8217+236delinsTG
XM_006724475.2:c.8217+235_8217+236delinsTG	XP_006724538.1:n.8217+235_8217+236delinsTG
XM_011545467.1:c.8094+235_8094+236delinsTG	XP_011543769.1:n.8094+235_8094+236delinsTG
XM_011545468.1:c.8217+235_8217+236delinsTG	XP_011543770.1:n.8217+235_8217+236delinsTG
XM_006724469.3:c.8193+235_8193+236delinsTG	XP_006724532.1:n.8193+235_8193+236delinsTG
XM_006724470.3:c.8217+235_8217+236delinsTG	XP_006724533.1:n.8217+235_8217+236delinsTG
XM_006724474.3:c.8217+235_8217+236delinsTG	XP_006724537.1:n.8217+235_8217+236delinsTG
XM_011545468.2:c.8217+235_8217+236delinsTG	XP_011543770.1:n.8217+235_8217+236delinsTG
XM_017029328.1:c.8217+235_8217+236delinsTG	XP_016884817.1:n.8217+235_8217+236delinsTG
XM_017029331.1:c.2391+235_2391+236delinsTG	XP_016884820.1:n.2391+235_2391+236delinsTG
NM_000109.4:c.8193+235_8193+236delinsTG	NP_000100.3:n.8193+235_8193+236delinsTG
NM_004006.3:c.8217+235_8217+236delinsTG MANE Select	NP_003997.2:n.8217+235_8217+236delinsTG
NM_004011.4:c.4194+235_4194+236delinsTG	NP_004002.3:n.4194+235_4194+236delinsTG
NM_004012.4:c.4185+235_4185+236delinsTG	NP_004003.2:n.4185+235_4185+236delinsTG
NM_004021.3:c.837+235_837+236delinsTG	NP_004012.2:n.837+235_837+236delinsTG
NM_004023.3:c.837+235_837+236delinsTG	NP_004014.2:n.837+235_837+236delinsTG
NM_004013.3:c.837+235_837+236delinsTG	NP_004004.2:n.837+235_837+236delinsTG
NM_004020.4:c.837+235_837+236delinsTG	NP_004011.3:n.837+235_837+236delinsTG
NM_004022.3:c.837+235_837+236delinsTG	NP_004013.2:n.837+235_837+236delinsTG