Canonical Allele Identifier: CA382909418

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968178A>G (hg19) ; chr11:g.119097468A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097468A>G , CM000673.2:g.119097468A>G	GRCh38
NC_000011.9:g.118968178A>G , CM000673.1:g.118968178A>G	GRCh37
NC_000011.8:g.118473388A>G	NCBI36
NG_008918.1:g.9608T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1059T>C
ENST00000524658.2:n.1040T>C
ENST00000530052.2:n.2046T>C
ENST00000682191.1:n.1506T>C
ENST00000682192.1:n.1203T>C
ENST00000682232.1:c.*623-171T>C	ENSP00000507302.1:n.*623-171T>C
ENST00000682326.1:c.918-171T>C	ENSP00000508129.1:n.918-171T>C
ENST00000682404.1:n.2102T>C
ENST00000682517.1:n.2405T>C
ENST00000682652.1:n.2275T>C
ENST00000682665.1:n.1701T>C
ENST00000682691.1:n.1701T>C
ENST00000682791.1:c.914T>C	ENSP00000507312.1:p.Leu305Ser
ENST00000682811.1:c.*52T>C	ENSP00000508196.1:n.*52T>C
ENST00000682883.1:n.1032-171T>C
ENST00000682946.1:c.*83T>C	ENSP00000506856.1:n.*83T>C
ENST00000683143.1:c.*706T>C	ENSP00000507168.1:n.*706T>C
ENST00000683373.1:n.1506T>C
ENST00000683558.1:n.1506T>C
ENST00000683567.1:n.1110T>C
ENST00000683955.1:n.1757T>C
ENST00000684142.1:c.*676T>C	ENSP00000508008.1:n.*676T>C
ENST00000684252.1:n.1398T>C
ENST00000684255.1:c.*706T>C	ENSP00000507398.1:n.*706T>C
ENST00000684315.1:n.1734T>C
ENST00000684345.1:c.*979T>C	ENSP00000507163.1:n.*979T>C
ENST00000684499.1:c.*1106T>C	ENSP00000506800.1:n.*1106T>C
ENST00000684682.1:c.*732T>C	ENSP00000507326.1:n.*732T>C
ENST00000354202.9:c.1001T>C MANE Select	ENSP00000346142.4:p.Leu334Ser
ENST00000636404.1:c.233-405T>C
ENST00000638850.1:c.505T>C
ENST00000639704.1:c.908T>C	ENSP00000491336.1:p.Leu303Ser
ENST00000640102.1:c.*654T>C	ENSP00000492027.1:n.*654T>C
ENST00000640747.1:c.*676T>C	ENSP00000492730.1:n.*676T>C
ENST00000354202.8:c.1001T>C	ENSP00000346142.4:p.Leu334Ser
ENST00000392834.7:c.*706T>C	ENSP00000376579.3:n.*706T>C
ENST00000409993.6:c.1001T>C	ENSP00000386597.2:p.Leu334Ser
ENST00000414373.5:c.*475-171T>C	ENSP00000402019.1:n.*475-171T>C
ENST00000442480.1:c.733T>C	ENSP00000406591.1:n.733T>C
ENST00000461999.1:n.1168T>C
ENST00000481084.5:n.1630T>C
ENST00000524658.1:n.306T>C
ENST00000525456.5:n.815T>C
NM_001382.3:c.1001T>C	NP_001373.2:p.Leu334Ser
XM_005271422.2:c.1001T>C	XP_005271479.1:p.Leu334Ser
XM_011542648.1:c.680T>C	XP_011540950.1:p.Leu227Ser
XR_947801.1:n.1165-171T>C
XM_005271422.3:c.1001T>C	XP_005271479.1:p.Leu334Ser
XM_011542648.2:c.680T>C	XP_011540950.1:p.Leu227Ser
XM_017017293.2:c.680T>C	XP_016872782.1:p.Leu227Ser
XM_017017294.2:c.*83T>C	XP_016872783.1:n.*83T>C
XM_017017295.1:c.485T>C	XP_016872784.1:p.Leu162Ser
XR_001747785.2:n.1035T>C
XR_947801.2:n.952-171T>C
NM_001382.4:c.1001T>C MANE Select	NP_001373.2:p.Leu334Ser