Canonical Allele Identifier: CA412671664

Gene: DMD

Linked Data

• MyVariant Identifiers: chrX:g.32382811A>G (hg19) ; chrX:g.32364694A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32364694A>G , CM000685.2:g.32364694A>G	GRCh38
NC_000023.10:g.32382811A>G , CM000685.1:g.32382811A>G	GRCh37
NC_000023.9:g.32292732A>G	NCBI36
NG_012232.1:g.979916T>C , LRG_199:g.979916T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000357033.9:c.5042T>C MANE Select	ENSP00000354923.3:p.Met1681Thr
ENST00000619831.5:c.1010T>C	ENSP00000479270.2:p.Met337Thr
ENST00000357033.8:c.5042T>C	ENSP00000354923.3:p.Met1681Thr
ENST00000378677.6:c.5030T>C	ENSP00000367948.2:p.Met1677Thr
ENST00000420596.5:c.290T>C	ENSP00000399897.1:p.Met97Thr
ENST00000448370.5:c.110T>C	ENSP00000388559.1:p.Met37Thr
ENST00000488902.5:n.336-147631T>C
ENST00000619831.4:c.5030T>C	ENSP00000479270.1:p.Met1677Thr
ENST00000620040.4:c.5042T>C	ENSP00000478150.1:p.Met1681Thr
NM_000109.3:c.5018T>C	NP_000100.2:p.Met1673Thr
NM_004006.2:c.5042T>C , LRG_199t1:c.5042T>C	NP_003997.1:p.Met1681Thr
NM_004009.3:c.5030T>C	NP_004000.1:p.Met1677Thr
NM_004010.3:c.4673T>C	NP_004001.1:p.Met1558Thr
NM_004011.3:c.1019T>C	NP_004002.2:p.Met340Thr
NM_004012.3:c.1010T>C	NP_004003.1:p.Met337Thr
XM_006724468.2:c.5042T>C	XP_006724531.1:p.Met1681Thr
XM_006724469.2:c.5018T>C	XP_006724532.1:p.Met1673Thr
XM_006724470.2:c.5042T>C	XP_006724533.1:p.Met1681Thr
XM_006724471.2:c.5042T>C	XP_006724534.1:p.Met1681Thr
XM_006724472.2:c.4913T>C	XP_006724535.1:p.Met1638Thr
XM_006724473.2:c.5042T>C	XP_006724536.1:p.Met1681Thr
XM_006724474.2:c.5042T>C	XP_006724537.1:p.Met1681Thr
XM_006724475.2:c.5042T>C	XP_006724538.1:p.Met1681Thr
XM_011545467.1:c.5042T>C	XP_011543769.1:p.Met1681Thr
XM_011545468.1:c.5042T>C	XP_011543770.1:p.Met1681Thr
XM_011545469.1:c.5042T>C	XP_011543771.1:p.Met1681Thr
XM_006724469.3:c.5018T>C	XP_006724532.1:p.Met1673Thr
XM_006724470.3:c.5042T>C	XP_006724533.1:p.Met1681Thr
XM_006724474.3:c.5042T>C	XP_006724537.1:p.Met1681Thr
XM_011545468.2:c.5042T>C	XP_011543770.1:p.Met1681Thr
XM_017029328.1:c.5042T>C	XP_016884817.1:p.Met1681Thr
XM_017029329.1:c.5042T>C	XP_016884818.1:p.Met1681Thr
XM_017029330.2:c.5042T>C	XP_016884819.1:p.Met1681Thr
NM_000109.4:c.5018T>C	NP_000100.3:p.Met1673Thr
NM_004006.3:c.5042T>C MANE Select	NP_003997.2:p.Met1681Thr
NM_004011.4:c.1019T>C	NP_004002.3:p.Met340Thr
NM_004012.4:c.1010T>C	NP_004003.2:p.Met337Thr