Canonical Allele Identifier: CA672381973

Gene: DPAGT1

Linked Data

• dbSNP Id: rs1444951406
• MyVariant Identifiers: chr11:g.118968090C>G (hg19) ; chr11:g.119097380C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097380C>G , CM000673.2:g.119097380C>G	GRCh38
NC_000011.9:g.118968090C>G , CM000673.1:g.118968090C>G	GRCh37
NC_000011.8:g.118473300C>G	NCBI36
NG_008918.1:g.9696G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1147G>C
ENST00000524658.2:n.1128G>C
ENST00000530052.2:n.2134G>C
ENST00000682191.1:n.1511-83G>C
ENST00000682192.1:n.1291G>C
ENST00000682232.1:c.*623-83G>C	ENSP00000507302.1:n.*623-83G>C
ENST00000682326.1:c.918-83G>C	ENSP00000508129.1:n.918-83G>C
ENST00000682404.1:n.2190G>C
ENST00000682517.1:n.2493G>C
ENST00000682652.1:n.2280-83G>C
ENST00000682665.1:n.1789G>C
ENST00000682691.1:n.1789G>C
ENST00000682791.1:c.919-83G>C	ENSP00000507312.1:n.919-83G>C
ENST00000682811.1:c.*57-83G>C	ENSP00000508196.1:n.*57-83G>C
ENST00000682883.1:n.1032-83G>C
ENST00000682946.1:c.*88-83G>C	ENSP00000506856.1:n.*88-83G>C
ENST00000683143.1:c.*711-83G>C	ENSP00000507168.1:n.*711-83G>C
ENST00000683373.1:n.1511-83G>C
ENST00000683558.1:n.1594G>C
ENST00000683567.1:n.1115-83G>C
ENST00000683955.1:n.1762-83G>C
ENST00000684142.1:c.*764G>C	ENSP00000508008.1:n.*764G>C
ENST00000684252.1:n.1486G>C
ENST00000684255.1:c.*794G>C	ENSP00000507398.1:n.*794G>C
ENST00000684315.1:n.1739-83G>C
ENST00000684345.1:c.*1067G>C	ENSP00000507163.1:n.*1067G>C
ENST00000684499.1:c.*1194G>C	ENSP00000506800.1:n.*1194G>C
ENST00000684682.1:c.*820G>C	ENSP00000507326.1:n.*820G>C
ENST00000354202.9:c.1006-83G>C MANE Select	ENSP00000346142.4:n.1006-83G>C
ENST00000636404.1:c.233-317G>C
ENST00000638850.1:c.528+65G>C
ENST00000639704.1:c.913-83G>C	ENSP00000491336.1:n.913-83G>C
ENST00000640102.1:c.*659-83G>C	ENSP00000492027.1:n.*659-83G>C
ENST00000640747.1:c.*681-83G>C	ENSP00000492730.1:n.*681-83G>C
ENST00000354202.8:c.1006-83G>C	ENSP00000346142.4:n.1006-83G>C
ENST00000392834.7:c.*711-83G>C	ENSP00000376579.3:n.*711-83G>C
ENST00000409993.6:c.1006-83G>C	ENSP00000386597.2:n.1006-83G>C
ENST00000414373.5:c.*475-83G>C	ENSP00000402019.1:n.*475-83G>C
ENST00000442480.1:c.738-83G>C	ENSP00000406591.1:n.738-83G>C
ENST00000461999.1:n.1256G>C
ENST00000481084.5:n.1635-83G>C
ENST00000524658.1:n.394G>C
ENST00000525456.5:n.903G>C
NM_001382.3:c.1006-83G>C	NP_001373.2:n.1006-83G>C
XM_005271422.2:c.1006-83G>C	XP_005271479.1:n.1006-83G>C
XM_011542648.1:c.685-83G>C	XP_011540950.1:n.685-83G>C
XR_947801.1:n.1165-83G>C
XM_005271422.3:c.1006-83G>C	XP_005271479.1:n.1006-83G>C
XM_011542648.2:c.685-83G>C	XP_011540950.1:n.685-83G>C
XM_017017293.2:c.685-83G>C	XP_016872782.1:n.685-83G>C
XM_017017294.2:c.*171G>C	XP_016872783.1:n.*171G>C
XM_017017295.1:c.490-83G>C	XP_016872784.1:n.490-83G>C
XR_001747785.2:n.1040-83G>C
XR_947801.2:n.952-83G>C
NM_001382.4:c.1006-83G>C MANE Select	NP_001373.2:n.1006-83G>C