Canonical Allele Identifier: CA382914233

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118971023A>G (hg19) ; chr11:g.119100313A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100313A>G , CM000673.2:g.119100313A>G	GRCh38
NC_000011.9:g.118971023A>G , CM000673.1:g.118971023A>G	GRCh37
NC_000011.8:g.118476233A>G	NCBI36
NG_008918.1:g.6763T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.768T>C
ENST00000530052.2:n.1334T>C
ENST00000682191.1:n.794T>C
ENST00000682192.1:n.794T>C
ENST00000682232.1:c.*297T>C	ENSP00000507302.1:n.*297T>C
ENST00000682326.1:c.592T>C	ENSP00000508129.1:p.Ser198Pro
ENST00000682404.1:n.1334T>C
ENST00000682517.1:n.1334T>C
ENST00000682652.1:n.1563T>C
ENST00000682665.1:n.989T>C
ENST00000682691.1:n.989T>C
ENST00000682791.1:c.505T>C	ENSP00000507312.1:p.Ser169Pro
ENST00000682811.1:c.592T>C	ENSP00000508196.1:p.Ser198Pro
ENST00000682883.1:n.895T>C
ENST00000682946.1:c.592T>C	ENSP00000506856.1:p.Ser198Pro
ENST00000683143.1:c.*297T>C	ENSP00000507168.1:n.*297T>C
ENST00000683373.1:n.794T>C
ENST00000683558.1:n.794T>C
ENST00000683567.1:n.819T>C
ENST00000683955.1:n.989T>C
ENST00000684142.1:c.*267T>C	ENSP00000508008.1:n.*267T>C
ENST00000684252.1:n.989T>C
ENST00000684255.1:c.*297T>C	ENSP00000507398.1:n.*297T>C
ENST00000684315.1:n.1325T>C
ENST00000684345.1:c.*267T>C	ENSP00000507163.1:n.*267T>C
ENST00000684499.1:c.*697T>C	ENSP00000506800.1:n.*697T>C
ENST00000684682.1:c.*20T>C	ENSP00000507326.1:n.*20T>C
ENST00000354202.9:c.592T>C MANE Select	ENSP00000346142.4:p.Ser198Pro
ENST00000636404.1:c.96T>C
ENST00000638850.1:c.96T>C
ENST00000639704.1:c.499T>C	ENSP00000491336.1:p.Ser167Pro
ENST00000640102.1:c.*245T>C	ENSP00000492027.1:n.*245T>C
ENST00000640747.1:c.*267T>C	ENSP00000492730.1:n.*267T>C
ENST00000354202.8:c.592T>C	ENSP00000346142.4:p.Ser198Pro
ENST00000392834.7:c.*297T>C	ENSP00000376579.3:n.*297T>C
ENST00000409993.6:c.592T>C	ENSP00000386597.2:p.Ser198Pro
ENST00000414373.5:c.*338T>C	ENSP00000402019.1:n.*338T>C
ENST00000442480.1:c.442T>C	ENSP00000406591.1:p.Ser148Pro
ENST00000461999.1:n.97T>C
ENST00000481084.5:n.1221T>C
ENST00000525456.5:n.595T>C
ENST00000530052.1:n.490T>C
ENST00000533687.1:n.604T>C
NM_001382.3:c.592T>C	NP_001373.2:p.Ser198Pro
XM_005271422.2:c.592T>C	XP_005271479.1:p.Ser198Pro
XM_011542648.1:c.271T>C	XP_011540950.1:p.Ser91Pro
XR_947801.1:n.1028T>C
XM_005271422.3:c.592T>C	XP_005271479.1:p.Ser198Pro
XM_011542648.2:c.271T>C	XP_011540950.1:p.Ser91Pro
XM_017017293.2:c.271T>C	XP_016872782.1:p.Ser91Pro
XM_017017294.2:c.592T>C	XP_016872783.1:p.Ser198Pro
XM_017017295.1:c.76T>C	XP_016872784.1:p.Ser26Pro
XR_001747785.2:n.815T>C
XR_947801.2:n.815T>C
NM_001382.4:c.592T>C MANE Select	NP_001373.2:p.Ser198Pro