Canonical Allele Identifier: CA382914226

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119100312-G-T
• MyVariant Identifiers: chr11:g.118971022G>T (hg19) ; chr11:g.119100312G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100312G>T , CM000673.2:g.119100312G>T	GRCh38
NC_000011.9:g.118971022G>T , CM000673.1:g.118971022G>T	GRCh37
NC_000011.8:g.118476232G>T	NCBI36
NG_008918.1:g.6764C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.769C>A
ENST00000530052.2:n.1335C>A
ENST00000682191.1:n.795C>A
ENST00000682192.1:n.795C>A
ENST00000682232.1:c.*298C>A	ENSP00000507302.1:n.*298C>A
ENST00000682326.1:c.593C>A	ENSP00000508129.1:p.Ser198Ter
ENST00000682404.1:n.1335C>A
ENST00000682517.1:n.1335C>A
ENST00000682652.1:n.1564C>A
ENST00000682665.1:n.990C>A
ENST00000682691.1:n.990C>A
ENST00000682791.1:c.506C>A	ENSP00000507312.1:p.Ser169Ter
ENST00000682811.1:c.593C>A	ENSP00000508196.1:p.Ser198Ter
ENST00000682883.1:n.896C>A
ENST00000682946.1:c.593C>A	ENSP00000506856.1:p.Ser198Ter
ENST00000683143.1:c.*298C>A	ENSP00000507168.1:n.*298C>A
ENST00000683373.1:n.795C>A
ENST00000683558.1:n.795C>A
ENST00000683567.1:n.820C>A
ENST00000683955.1:n.990C>A
ENST00000684142.1:c.*268C>A	ENSP00000508008.1:n.*268C>A
ENST00000684252.1:n.990C>A
ENST00000684255.1:c.*298C>A	ENSP00000507398.1:n.*298C>A
ENST00000684315.1:n.1326C>A
ENST00000684345.1:c.*268C>A	ENSP00000507163.1:n.*268C>A
ENST00000684499.1:c.*698C>A	ENSP00000506800.1:n.*698C>A
ENST00000684682.1:c.*21C>A	ENSP00000507326.1:n.*21C>A
ENST00000354202.9:c.593C>A MANE Select	ENSP00000346142.4:p.Ser198Ter
ENST00000636404.1:c.97C>A
ENST00000638850.1:c.97C>A
ENST00000639704.1:c.500C>A	ENSP00000491336.1:p.Ser167Ter
ENST00000640102.1:c.*246C>A	ENSP00000492027.1:n.*246C>A
ENST00000640747.1:c.*268C>A	ENSP00000492730.1:n.*268C>A
ENST00000354202.8:c.593C>A	ENSP00000346142.4:p.Ser198Ter
ENST00000392834.7:c.*298C>A	ENSP00000376579.3:n.*298C>A
ENST00000409993.6:c.593C>A	ENSP00000386597.2:p.Ser198Ter
ENST00000414373.5:c.*339C>A	ENSP00000402019.1:n.*339C>A
ENST00000442480.1:c.443C>A	ENSP00000406591.1:p.Ser148Ter
ENST00000461999.1:n.98C>A
ENST00000481084.5:n.1222C>A
ENST00000525456.5:n.596C>A
ENST00000530052.1:n.491C>A
ENST00000533687.1:n.605C>A
NM_001382.3:c.593C>A	NP_001373.2:p.Ser198Ter
XM_005271422.2:c.593C>A	XP_005271479.1:p.Ser198Ter
XM_011542648.1:c.272C>A	XP_011540950.1:p.Ser91Ter
XR_947801.1:n.1029C>A
XM_005271422.3:c.593C>A	XP_005271479.1:p.Ser198Ter
XM_011542648.2:c.272C>A	XP_011540950.1:p.Ser91Ter
XM_017017293.2:c.272C>A	XP_016872782.1:p.Ser91Ter
XM_017017294.2:c.593C>A	XP_016872783.1:p.Ser198Ter
XM_017017295.1:c.77C>A	XP_016872784.1:p.Ser26Ter
XR_001747785.2:n.816C>A
XR_947801.2:n.816C>A
NM_001382.4:c.593C>A MANE Select	NP_001373.2:p.Ser198Ter