Canonical Allele Identifier: CA382908984

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118967986C>T (hg19) ; chr11:g.119097276C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097276C>T , CM000673.2:g.119097276C>T	GRCh38
NC_000011.9:g.118967986C>T , CM000673.1:g.118967986C>T	GRCh37
NC_000011.8:g.118473196C>T	NCBI36
NG_008918.1:g.9800G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1251G>A
ENST00000524658.2:n.1232G>A
ENST00000530052.2:n.2238G>A
ENST00000682191.1:n.1532G>A
ENST00000682192.1:n.1395G>A
ENST00000682232.1:c.*644G>A	ENSP00000507302.1:n.*644G>A
ENST00000682326.1:c.939G>A	ENSP00000508129.1:p.Trp313Ter
ENST00000682404.1:n.2294G>A
ENST00000682517.1:n.2597G>A
ENST00000682652.1:n.2301G>A
ENST00000682665.1:n.1893G>A
ENST00000682691.1:n.1893G>A
ENST00000682791.1:c.940G>A	ENSP00000507312.1:p.Val314Met
ENST00000682811.1:c.*78G>A	ENSP00000508196.1:n.*78G>A
ENST00000682883.1:n.1053G>A
ENST00000682946.1:c.*109G>A	ENSP00000506856.1:n.*109G>A
ENST00000683143.1:c.*732G>A	ENSP00000507168.1:n.*732G>A
ENST00000683373.1:n.1532G>A
ENST00000683558.1:n.1698G>A
ENST00000683567.1:n.1136G>A
ENST00000683955.1:n.1783G>A
ENST00000684142.1:c.*868G>A	ENSP00000508008.1:n.*868G>A
ENST00000684252.1:n.1590G>A
ENST00000684255.1:c.*898G>A	ENSP00000507398.1:n.*898G>A
ENST00000684315.1:n.1760G>A
ENST00000684345.1:c.*1171G>A	ENSP00000507163.1:n.*1171G>A
ENST00000684499.1:c.*1298G>A	ENSP00000506800.1:n.*1298G>A
ENST00000684682.1:c.*924G>A	ENSP00000507326.1:n.*924G>A
ENST00000354202.9:c.1027G>A MANE Select	ENSP00000346142.4:p.Val343Met
ENST00000636404.1:c.233-213G>A
ENST00000638850.1:c.550G>A
ENST00000639704.1:c.934G>A	ENSP00000491336.1:p.Val312Met
ENST00000640102.1:c.*680G>A	ENSP00000492027.1:n.*680G>A
ENST00000640747.1:c.*702G>A	ENSP00000492730.1:n.*702G>A
ENST00000354202.8:c.1027G>A	ENSP00000346142.4:p.Val343Met
ENST00000392834.7:c.*732G>A	ENSP00000376579.3:n.*732G>A
ENST00000409993.6:c.1027G>A	ENSP00000386597.2:p.Val343Met
ENST00000414373.5:c.*496G>A	ENSP00000402019.1:n.*496G>A
ENST00000442480.1:c.759G>A	ENSP00000406591.1:n.759G>A
ENST00000461999.1:n.1360G>A
ENST00000481084.5:n.1656G>A
ENST00000525456.5:n.1007G>A
NM_001382.3:c.1027G>A	NP_001373.2:p.Val343Met
XM_005271422.2:c.1027G>A	XP_005271479.1:p.Val343Met
XM_011542648.1:c.706G>A	XP_011540950.1:p.Val236Met
XR_947801.1:n.1186G>A
XM_005271422.3:c.1027G>A	XP_005271479.1:p.Val343Met
XM_011542648.2:c.706G>A	XP_011540950.1:p.Val236Met
XM_017017293.2:c.706G>A	XP_016872782.1:p.Val236Met
XM_017017294.2:c.*275G>A	XP_016872783.1:n.*275G>A
XM_017017295.1:c.511G>A	XP_016872784.1:p.Val171Met
XR_001747785.2:n.1061G>A
XR_947801.2:n.973G>A
NM_001382.4:c.1027G>A MANE Select	NP_001373.2:p.Val343Met