Canonical Allele Identifier: CA2422736310

Gene: DMD

Linked Data

• dbSNP Id: rs2097445984

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32287268_32287269del , CM000685.2:g.32287268_32287269del	GRCh38
NC_000023.10:g.32305385_32305386del , CM000685.1:g.32305385_32305386del	GRCh37
NC_000023.9:g.32215306_32215307del	NCBI36
NG_012232.1:g.1057342_1057343del , LRG_199:g.1057342_1057343del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000358062.7:c.1136+261_1136+262del	ENSP00000350765.3:n.1136+261_1136+262del
ENST00000357033.9:c.6290+261_6290+262del MANE Select	ENSP00000354923.3:n.6290+261_6290+262del
ENST00000619831.5:c.2258+261_2258+262del	ENSP00000479270.2:n.2258+261_2258+262del
ENST00000357033.8:c.6290+261_6290+262del	ENSP00000354923.3:n.6290+261_6290+262del
ENST00000378677.6:c.6278+261_6278+262del	ENSP00000367948.2:n.6278+261_6278+262del
ENST00000488902.5:n.336-70205_336-70204del
ENST00000619831.4:c.6278+261_6278+262del	ENSP00000479270.1:n.6278+261_6278+262del
ENST00000620040.4:c.6290+261_6290+262del	ENSP00000478150.1:n.6290+261_6290+262del
NM_000109.3:c.6266+261_6266+262del	NP_000100.2:n.6266+261_6266+262del
NM_004006.2:c.6290+261_6290+262del , LRG_199t1:c.6290+261_6290+262del	NP_003997.1:n.6290+261_6290+262del
NM_004009.3:c.6278+261_6278+262del	NP_004000.1:n.6278+261_6278+262del
NM_004010.3:c.5921+261_5921+262del	NP_004001.1:n.5921+261_5921+262del
NM_004011.3:c.2267+261_2267+262del	NP_004002.2:n.2267+261_2267+262del
NM_004012.3:c.2258+261_2258+262del	NP_004003.1:n.2258+261_2258+262del
XM_006724468.2:c.6290+261_6290+262del	XP_006724531.1:n.6290+261_6290+262del
XM_006724469.2:c.6266+261_6266+262del	XP_006724532.1:n.6266+261_6266+262del
XM_006724470.2:c.6290+261_6290+262del	XP_006724533.1:n.6290+261_6290+262del
XM_006724471.2:c.6290+261_6290+262del	XP_006724534.1:n.6290+261_6290+262del
XM_006724472.2:c.6161+261_6161+262del	XP_006724535.1:n.6161+261_6161+262del
XM_006724473.2:c.6152+261_6152+262del	XP_006724536.1:n.6152+261_6152+262del
XM_006724474.2:c.6290+261_6290+262del	XP_006724537.1:n.6290+261_6290+262del
XM_006724475.2:c.6290+261_6290+262del	XP_006724538.1:n.6290+261_6290+262del
XM_011545467.1:c.6167+261_6167+262del	XP_011543769.1:n.6167+261_6167+262del
XM_011545468.1:c.6290+261_6290+262del	XP_011543770.1:n.6290+261_6290+262del
XM_006724469.3:c.6266+261_6266+262del	XP_006724532.1:n.6266+261_6266+262del
XM_006724470.3:c.6290+261_6290+262del	XP_006724533.1:n.6290+261_6290+262del
XM_006724474.3:c.6290+261_6290+262del	XP_006724537.1:n.6290+261_6290+262del
XM_011545468.2:c.6290+261_6290+262del	XP_011543770.1:n.6290+261_6290+262del
XM_017029328.1:c.6290+261_6290+262del	XP_016884817.1:n.6290+261_6290+262del
XM_017029329.1:c.6290+261_6290+262del	XP_016884818.1:n.6290+261_6290+262del
XM_017029330.2:c.6290+261_6290+262del	XP_016884819.1:n.6290+261_6290+262del
XM_017029331.1:c.464+261_464+262del	XP_016884820.1:n.464+261_464+262del
NM_000109.4:c.6266+261_6266+262del	NP_000100.3:n.6266+261_6266+262del
NM_004006.3:c.6290+261_6290+262del MANE Select	NP_003997.2:n.6290+261_6290+262del
NM_004011.4:c.2267+261_2267+262del	NP_004002.3:n.2267+261_2267+262del
NM_004012.4:c.2258+261_2258+262del	NP_004003.2:n.2258+261_2258+262del