Canonical Allele Identifier: CA412671572

Gene: DMD

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32364655C>T , CM000685.2:g.32364655C>T	GRCh38
NC_000023.10:g.32382772C>T , CM000685.1:g.32382772C>T	GRCh37
NC_000023.9:g.32292693C>T	NCBI36
NG_012232.1:g.979955G>A , LRG_199:g.979955G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_004006.3:c.5081G>A MANE Select	NP_003997.2:p.Trp1694Ter
ENST00000357033.9:c.5081G>A MANE Select	ENSP00000354923.3:p.Trp1694Ter
NM_000109.3:c.5057G>A	NP_000100.2:p.Trp1686Ter
NM_000109.4:c.5057G>A	NP_000100.3:p.Trp1686Ter
NM_004006.2:c.5081G>A , LRG_199t1:c.5081G>A	NP_003997.1:p.Trp1694Ter
NM_004009.3:c.5069G>A	NP_004000.1:p.Trp1690Ter
NM_004010.3:c.4712G>A	NP_004001.1:p.Trp1571Ter
NM_004011.3:c.1058G>A	NP_004002.2:p.Trp353Ter
NM_004011.4:c.1058G>A	NP_004002.3:p.Trp353Ter
NM_004012.3:c.1049G>A	NP_004003.1:p.Trp350Ter
NM_004012.4:c.1049G>A	NP_004003.2:p.Trp350Ter
ENST00000357033.8:c.5081G>A	ENSP00000354923.3:p.Trp1694Ter
ENST00000378677.6:c.5069G>A	ENSP00000367948.2:p.Trp1690Ter
ENST00000488902.5:n.336-147592G>A
ENST00000619831.4:c.5069G>A	ENSP00000479270.1:p.Trp1690Ter
ENST00000619831.5:c.1049G>A	ENSP00000479270.2:p.Trp350Ter
ENST00000620040.4:c.5081G>A	ENSP00000478150.1:p.Trp1694Ter
XM_006724468.2:c.5081G>A	XP_006724531.1:p.Trp1694Ter
XM_006724469.2:c.5057G>A	XP_006724532.1:p.Trp1686Ter
XM_006724469.3:c.5057G>A	XP_006724532.1:p.Trp1686Ter
XM_006724470.2:c.5081G>A	XP_006724533.1:p.Trp1694Ter
XM_006724470.3:c.5081G>A	XP_006724533.1:p.Trp1694Ter
XM_006724471.2:c.5081G>A	XP_006724534.1:p.Trp1694Ter
XM_006724472.2:c.4952G>A	XP_006724535.1:p.Trp1651Ter
XM_006724473.2:c.5081G>A	XP_006724536.1:p.Trp1694Ter
XM_006724474.2:c.5081G>A	XP_006724537.1:p.Trp1694Ter
XM_006724474.3:c.5081G>A	XP_006724537.1:p.Trp1694Ter
XM_006724475.2:c.5081G>A	XP_006724538.1:p.Trp1694Ter
XM_011545467.1:c.5081G>A	XP_011543769.1:p.Trp1694Ter
XM_011545468.1:c.5081G>A	XP_011543770.1:p.Trp1694Ter
XM_011545468.2:c.5081G>A	XP_011543770.1:p.Trp1694Ter
XM_011545469.1:c.5081G>A	XP_011543771.1:p.Trp1694Ter
XM_017029328.1:c.5081G>A	XP_016884817.1:p.Trp1694Ter
XM_017029329.1:c.5081G>A	XP_016884818.1:p.Trp1694Ter
XM_017029330.2:c.5081G>A	XP_016884819.1:p.Trp1694Ter