Canonical Allele Identifier: CA672381971

Gene: DPAGT1

Linked Data

• dbSNP Id: rs1194788035
• MyVariant Identifiers: chr11:g.118968085T>C (hg19) ; chr11:g.119097375T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097375T>C , CM000673.2:g.119097375T>C	GRCh38
NC_000011.9:g.118968085T>C , CM000673.1:g.118968085T>C	GRCh37
NC_000011.8:g.118473295T>C	NCBI36
NG_008918.1:g.9701A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1152A>G
ENST00000524658.2:n.1133A>G
ENST00000530052.2:n.2139A>G
ENST00000682191.1:n.1511-78A>G
ENST00000682192.1:n.1296A>G
ENST00000682232.1:c.*623-78A>G	ENSP00000507302.1:n.*623-78A>G
ENST00000682326.1:c.918-78A>G	ENSP00000508129.1:n.918-78A>G
ENST00000682404.1:n.2195A>G
ENST00000682517.1:n.2498A>G
ENST00000682652.1:n.2280-78A>G
ENST00000682665.1:n.1794A>G
ENST00000682691.1:n.1794A>G
ENST00000682791.1:c.919-78A>G	ENSP00000507312.1:n.919-78A>G
ENST00000682811.1:c.*57-78A>G	ENSP00000508196.1:n.*57-78A>G
ENST00000682883.1:n.1032-78A>G
ENST00000682946.1:c.*88-78A>G	ENSP00000506856.1:n.*88-78A>G
ENST00000683143.1:c.*711-78A>G	ENSP00000507168.1:n.*711-78A>G
ENST00000683373.1:n.1511-78A>G
ENST00000683558.1:n.1599A>G
ENST00000683567.1:n.1115-78A>G
ENST00000683955.1:n.1762-78A>G
ENST00000684142.1:c.*769A>G	ENSP00000508008.1:n.*769A>G
ENST00000684252.1:n.1491A>G
ENST00000684255.1:c.*799A>G	ENSP00000507398.1:n.*799A>G
ENST00000684315.1:n.1739-78A>G
ENST00000684345.1:c.*1072A>G	ENSP00000507163.1:n.*1072A>G
ENST00000684499.1:c.*1199A>G	ENSP00000506800.1:n.*1199A>G
ENST00000684682.1:c.*825A>G	ENSP00000507326.1:n.*825A>G
ENST00000354202.9:c.1006-78A>G MANE Select	ENSP00000346142.4:n.1006-78A>G
ENST00000636404.1:c.233-312A>G
ENST00000638850.1:c.528+70A>G
ENST00000639704.1:c.913-78A>G	ENSP00000491336.1:n.913-78A>G
ENST00000640102.1:c.*659-78A>G	ENSP00000492027.1:n.*659-78A>G
ENST00000640747.1:c.*681-78A>G	ENSP00000492730.1:n.*681-78A>G
ENST00000354202.8:c.1006-78A>G	ENSP00000346142.4:n.1006-78A>G
ENST00000392834.7:c.*711-78A>G	ENSP00000376579.3:n.*711-78A>G
ENST00000409993.6:c.1006-78A>G	ENSP00000386597.2:n.1006-78A>G
ENST00000414373.5:c.*475-78A>G	ENSP00000402019.1:n.*475-78A>G
ENST00000442480.1:c.738-78A>G	ENSP00000406591.1:n.738-78A>G
ENST00000461999.1:n.1261A>G
ENST00000481084.5:n.1635-78A>G
ENST00000524658.1:n.399A>G
ENST00000525456.5:n.908A>G
NM_001382.3:c.1006-78A>G	NP_001373.2:n.1006-78A>G
XM_005271422.2:c.1006-78A>G	XP_005271479.1:n.1006-78A>G
XM_011542648.1:c.685-78A>G	XP_011540950.1:n.685-78A>G
XR_947801.1:n.1165-78A>G
XM_005271422.3:c.1006-78A>G	XP_005271479.1:n.1006-78A>G
XM_011542648.2:c.685-78A>G	XP_011540950.1:n.685-78A>G
XM_017017293.2:c.685-78A>G	XP_016872782.1:n.685-78A>G
XM_017017294.2:c.*176A>G	XP_016872783.1:n.*176A>G
XM_017017295.1:c.490-78A>G	XP_016872784.1:n.490-78A>G
XR_001747785.2:n.1040-78A>G
XR_947801.2:n.952-78A>G
NM_001382.4:c.1006-78A>G MANE Select	NP_001373.2:n.1006-78A>G