Canonical Allele Identifier: CA327995616

Gene: DMD

Linked Data

• dbSNP Id: rs745465665
• gnomAD v4: X-32365055-T-C
• MyVariant Identifiers: chrX:g.32383172T>C (hg19) ; chrX:g.32365055T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.32365055T>C , CM000685.2:g.32365055T>C	GRCh38
NC_000023.10:g.32383172T>C , CM000685.1:g.32383172T>C	GRCh37
NC_000023.9:g.32293093T>C	NCBI36
NG_012232.1:g.979555A>G , LRG_199:g.979555A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357033.9:c.4990A>G MANE Select	ENSP00000354923.3:p.Thr1664Ala
ENST00000619831.5:c.958A>G	ENSP00000479270.2:p.Thr320Ala
ENST00000357033.8:c.4990A>G	ENSP00000354923.3:p.Thr1664Ala
ENST00000378677.6:c.4978A>G	ENSP00000367948.2:p.Thr1660Ala
ENST00000420596.5:c.238A>G	ENSP00000399897.1:p.Thr80Ala
ENST00000448370.5:c.94-345A>G	ENSP00000388559.1:n.94-345A>G
ENST00000488902.5:n.336-147992A>G
ENST00000619831.4:c.4978A>G	ENSP00000479270.1:p.Thr1660Ala
ENST00000620040.4:c.4990A>G	ENSP00000478150.1:p.Thr1664Ala
NM_000109.3:c.4966A>G	NP_000100.2:p.Thr1656Ala
NM_004006.2:c.4990A>G , LRG_199t1:c.4990A>G	NP_003997.1:p.Thr1664Ala
NM_004009.3:c.4978A>G	NP_004000.1:p.Thr1660Ala
NM_004010.3:c.4621A>G	NP_004001.1:p.Thr1541Ala
NM_004011.3:c.967A>G	NP_004002.2:p.Thr323Ala
NM_004012.3:c.958A>G	NP_004003.1:p.Thr320Ala
XM_006724468.2:c.4990A>G	XP_006724531.1:p.Thr1664Ala
XM_006724469.2:c.4966A>G	XP_006724532.1:p.Thr1656Ala
XM_006724470.2:c.4990A>G	XP_006724533.1:p.Thr1664Ala
XM_006724471.2:c.4990A>G	XP_006724534.1:p.Thr1664Ala
XM_006724472.2:c.4861A>G	XP_006724535.1:p.Thr1621Ala
XM_006724473.2:c.4990A>G	XP_006724536.1:p.Thr1664Ala
XM_006724474.2:c.4990A>G	XP_006724537.1:p.Thr1664Ala
XM_006724475.2:c.4990A>G	XP_006724538.1:p.Thr1664Ala
XM_011545467.1:c.4990A>G	XP_011543769.1:p.Thr1664Ala
XM_011545468.1:c.4990A>G	XP_011543770.1:p.Thr1664Ala
XM_011545469.1:c.4990A>G	XP_011543771.1:p.Thr1664Ala
XM_006724469.3:c.4966A>G	XP_006724532.1:p.Thr1656Ala
XM_006724470.3:c.4990A>G	XP_006724533.1:p.Thr1664Ala
XM_006724474.3:c.4990A>G	XP_006724537.1:p.Thr1664Ala
XM_011545468.2:c.4990A>G	XP_011543770.1:p.Thr1664Ala
XM_017029328.1:c.4990A>G	XP_016884817.1:p.Thr1664Ala
XM_017029329.1:c.4990A>G	XP_016884818.1:p.Thr1664Ala
XM_017029330.2:c.4990A>G	XP_016884819.1:p.Thr1664Ala
NM_000109.4:c.4966A>G	NP_000100.3:p.Thr1656Ala
NM_004006.3:c.4990A>G MANE Select	NP_003997.2:p.Thr1664Ala
NM_004011.4:c.967A>G	NP_004002.3:p.Thr323Ala
NM_004012.4:c.958A>G	NP_004003.2:p.Thr320Ala