Canonical Allele Identifier: CA6314501

Gene: DPAGT1

Linked Data

• dbSNP Id: rs528948285
• ExAC: 11:118968296 A / G
• gnomAD v2: 11-118968296-A-G
• gnomAD v3: 11-119097586-A-G
• gnomAD v4: 11-119097586-A-G
• MyVariant Identifiers: chr11:g.118968296A>G (hg19) ; chr11:g.119097586A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097586A>G , CM000673.2:g.119097586A>G	GRCh38
NC_000011.9:g.118968296A>G , CM000673.1:g.118968296A>G	GRCh37
NC_000011.8:g.118473506A>G	NCBI36
NG_008918.1:g.9490T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-35T>C
ENST00000524658.2:n.957-35T>C
ENST00000530052.2:n.1928T>C
ENST00000682191.1:n.1388T>C
ENST00000682192.1:n.1120-35T>C
ENST00000682232.1:c.*622+269T>C	ENSP00000507302.1:n.*622+269T>C
ENST00000682326.1:c.917+269T>C	ENSP00000508129.1:n.917+269T>C
ENST00000682404.1:n.2019-35T>C
ENST00000682517.1:n.2287T>C
ENST00000682652.1:n.2157T>C
ENST00000682665.1:n.1583T>C
ENST00000682691.1:n.1583T>C
ENST00000682791.1:c.831-35T>C	ENSP00000507312.1:n.831-35T>C
ENST00000682811.1:c.800-35T>C	ENSP00000508196.1:n.800-35T>C
ENST00000682883.1:n.1032-289T>C
ENST00000682946.1:c.729-35T>C	ENSP00000506856.1:n.729-35T>C
ENST00000683143.1:c.*623-35T>C	ENSP00000507168.1:n.*623-35T>C
ENST00000683373.1:n.1388T>C
ENST00000683558.1:n.1388T>C
ENST00000683567.1:n.1027-35T>C
ENST00000683955.1:n.1674-35T>C
ENST00000684142.1:c.*593-35T>C	ENSP00000508008.1:n.*593-35T>C
ENST00000684252.1:n.1315-35T>C
ENST00000684255.1:c.*623-35T>C	ENSP00000507398.1:n.*623-35T>C
ENST00000684315.1:n.1651-35T>C
ENST00000684345.1:c.*861T>C	ENSP00000507163.1:n.*861T>C
ENST00000684499.1:c.*1023-35T>C	ENSP00000506800.1:n.*1023-35T>C
ENST00000684682.1:c.*614T>C	ENSP00000507326.1:n.*614T>C
ENST00000354202.9:c.918-35T>C MANE Select	ENSP00000346142.4:n.918-35T>C
ENST00000636404.1:c.233-523T>C
ENST00000638850.1:c.422-35T>C
ENST00000639704.1:c.825-35T>C	ENSP00000491336.1:n.825-35T>C
ENST00000640102.1:c.*571-35T>C	ENSP00000492027.1:n.*571-35T>C
ENST00000640747.1:c.*593-35T>C	ENSP00000492730.1:n.*593-35T>C
ENST00000354202.8:c.918-35T>C	ENSP00000346142.4:n.918-35T>C
ENST00000392834.7:c.*623-35T>C	ENSP00000376579.3:n.*623-35T>C
ENST00000409993.6:c.918-35T>C	ENSP00000386597.2:n.918-35T>C
ENST00000414373.5:c.*475-289T>C	ENSP00000402019.1:n.*475-289T>C
ENST00000442480.1:c.650-35T>C	ENSP00000406591.1:n.650-35T>C
ENST00000461999.1:n.1050T>C
ENST00000481084.5:n.1547-35T>C
ENST00000524658.1:n.223-35T>C
ENST00000525456.5:n.732-35T>C
NM_001382.3:c.918-35T>C	NP_001373.2:n.918-35T>C
XM_005271422.2:c.918-35T>C	XP_005271479.1:n.918-35T>C
XM_011542648.1:c.597-35T>C	XP_011540950.1:n.597-35T>C
XR_947801.1:n.1165-289T>C
XM_005271422.3:c.918-35T>C	XP_005271479.1:n.918-35T>C
XM_011542648.2:c.597-35T>C	XP_011540950.1:n.597-35T>C
XM_017017293.2:c.597-35T>C	XP_016872782.1:n.597-35T>C
XM_017017294.2:c.729-35T>C	XP_016872783.1:n.729-35T>C
XM_017017295.1:c.402-35T>C	XP_016872784.1:n.402-35T>C
XR_001747785.2:n.952-35T>C
XR_947801.2:n.952-289T>C
NM_001382.4:c.918-35T>C MANE Select	NP_001373.2:n.918-35T>C