Canonical Allele Identifier: CA382914235

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118971024C>A (hg19) ; chr11:g.119100314C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100314C>A , CM000673.2:g.119100314C>A	GRCh38
NC_000011.9:g.118971024C>A , CM000673.1:g.118971024C>A	GRCh37
NC_000011.8:g.118476234C>A	NCBI36
NG_008918.1:g.6762G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.767G>T
ENST00000530052.2:n.1333G>T
ENST00000682191.1:n.793G>T
ENST00000682192.1:n.793G>T
ENST00000682232.1:c.*296G>T	ENSP00000507302.1:n.*296G>T
ENST00000682326.1:c.591G>T	ENSP00000508129.1:p.Gln197His
ENST00000682404.1:n.1333G>T
ENST00000682517.1:n.1333G>T
ENST00000682652.1:n.1562G>T
ENST00000682665.1:n.988G>T
ENST00000682691.1:n.988G>T
ENST00000682791.1:c.504G>T	ENSP00000507312.1:p.Gln168His
ENST00000682811.1:c.591G>T	ENSP00000508196.1:p.Gln197His
ENST00000682883.1:n.894G>T
ENST00000682946.1:c.591G>T	ENSP00000506856.1:p.Gln197His
ENST00000683143.1:c.*296G>T	ENSP00000507168.1:n.*296G>T
ENST00000683373.1:n.793G>T
ENST00000683558.1:n.793G>T
ENST00000683567.1:n.818G>T
ENST00000683955.1:n.988G>T
ENST00000684142.1:c.*266G>T	ENSP00000508008.1:n.*266G>T
ENST00000684252.1:n.988G>T
ENST00000684255.1:c.*296G>T	ENSP00000507398.1:n.*296G>T
ENST00000684315.1:n.1324G>T
ENST00000684345.1:c.*266G>T	ENSP00000507163.1:n.*266G>T
ENST00000684499.1:c.*696G>T	ENSP00000506800.1:n.*696G>T
ENST00000684682.1:c.*19G>T	ENSP00000507326.1:n.*19G>T
ENST00000354202.9:c.591G>T MANE Select	ENSP00000346142.4:p.Gln197His
ENST00000636404.1:c.95G>T
ENST00000638850.1:c.95G>T
ENST00000639704.1:c.498G>T	ENSP00000491336.1:p.Gln166His
ENST00000640102.1:c.*244G>T	ENSP00000492027.1:n.*244G>T
ENST00000640747.1:c.*266G>T	ENSP00000492730.1:n.*266G>T
ENST00000354202.8:c.591G>T	ENSP00000346142.4:p.Gln197His
ENST00000392834.7:c.*296G>T	ENSP00000376579.3:n.*296G>T
ENST00000409993.6:c.591G>T	ENSP00000386597.2:p.Gln197His
ENST00000414373.5:c.*337G>T	ENSP00000402019.1:n.*337G>T
ENST00000442480.1:c.441G>T	ENSP00000406591.1:p.Gln147His
ENST00000461999.1:n.96G>T
ENST00000481084.5:n.1220G>T
ENST00000525456.5:n.594G>T
ENST00000530052.1:n.489G>T
ENST00000533687.1:n.603G>T
NM_001382.3:c.591G>T	NP_001373.2:p.Gln197His
XM_005271422.2:c.591G>T	XP_005271479.1:p.Gln197His
XM_011542648.1:c.270G>T	XP_011540950.1:p.Gln90His
XR_947801.1:n.1027G>T
XM_005271422.3:c.591G>T	XP_005271479.1:p.Gln197His
XM_011542648.2:c.270G>T	XP_011540950.1:p.Gln90His
XM_017017293.2:c.270G>T	XP_016872782.1:p.Gln90His
XM_017017294.2:c.591G>T	XP_016872783.1:p.Gln197His
XM_017017295.1:c.75G>T	XP_016872784.1:p.Gln25His
XR_001747785.2:n.814G>T
XR_947801.2:n.814G>T
NM_001382.4:c.591G>T MANE Select	NP_001373.2:p.Gln197His