Canonical Allele Identifier: CA477369789

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968258G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097548G>A , CM000673.2:g.119097548G>A	GRCh38
NC_000011.9:g.118968258G>A , CM000673.1:g.118968258G>A	GRCh37
NC_000011.8:g.118473468G>A	NCBI36
NG_008918.1:g.9528C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.979C>T
ENST00000524658.2:n.960C>T
ENST00000530052.2:n.1966C>T
ENST00000682191.1:n.1426C>T
ENST00000682192.1:n.1123C>T
ENST00000682232.1:c.*623-251C>T	ENSP00000507302.1:n.*623-251C>T
ENST00000682326.1:c.918-251C>T	ENSP00000508129.1:n.918-251C>T
ENST00000682404.1:n.2022C>T
ENST00000682517.1:n.2325C>T
ENST00000682652.1:n.2195C>T
ENST00000682665.1:n.1621C>T
ENST00000682691.1:n.1621C>T
ENST00000682791.1:c.834C>T	ENSP00000507312.1:p.Leu278=
ENST00000682811.1:c.803C>T	ENSP00000508196.1:p.Ser268Leu
ENST00000682883.1:n.1032-251C>T
ENST00000682946.1:c.*3C>T	ENSP00000506856.1:n.*3C>T
ENST00000683143.1:c.*626C>T	ENSP00000507168.1:n.*626C>T
ENST00000683373.1:n.1426C>T
ENST00000683558.1:n.1426C>T
ENST00000683567.1:n.1030C>T
ENST00000683955.1:n.1677C>T
ENST00000684142.1:c.*596C>T	ENSP00000508008.1:n.*596C>T
ENST00000684252.1:n.1318C>T
ENST00000684255.1:c.*626C>T	ENSP00000507398.1:n.*626C>T
ENST00000684315.1:n.1654C>T
ENST00000684345.1:c.*899C>T	ENSP00000507163.1:n.*899C>T
ENST00000684499.1:c.*1026C>T	ENSP00000506800.1:n.*1026C>T
ENST00000684682.1:c.*652C>T	ENSP00000507326.1:n.*652C>T
ENST00000354202.9:c.921C>T MANE Select	ENSP00000346142.4:p.Leu307=
ENST00000636404.1:c.233-485C>T
ENST00000638850.1:c.425C>T
ENST00000639704.1:c.828C>T	ENSP00000491336.1:p.Leu276=
ENST00000640102.1:c.*574C>T	ENSP00000492027.1:n.*574C>T
ENST00000640747.1:c.*596C>T	ENSP00000492730.1:n.*596C>T
ENST00000354202.8:c.921C>T	ENSP00000346142.4:p.Leu307=
ENST00000392834.7:c.*626C>T	ENSP00000376579.3:n.*626C>T
ENST00000409993.6:c.921C>T	ENSP00000386597.2:p.Leu307=
ENST00000414373.5:c.*475-251C>T	ENSP00000402019.1:n.*475-251C>T
ENST00000442480.1:c.653C>T	ENSP00000406591.1:p.Ser218Leu
ENST00000461999.1:n.1088C>T
ENST00000481084.5:n.1550C>T
ENST00000524658.1:n.226C>T
ENST00000525456.5:n.735C>T
NM_001382.3:c.921C>T	NP_001373.2:p.Leu307=
XM_005271422.2:c.921C>T	XP_005271479.1:p.Leu307=
XM_011542648.1:c.600C>T	XP_011540950.1:p.Leu200=
XR_947801.1:n.1165-251C>T
XM_005271422.3:c.921C>T	XP_005271479.1:p.Leu307=
XM_011542648.2:c.600C>T	XP_011540950.1:p.Leu200=
XM_017017293.2:c.600C>T	XP_016872782.1:p.Leu200=
XM_017017294.2:c.*3C>T	XP_016872783.1:n.*3C>T
XM_017017295.1:c.405C>T	XP_016872784.1:p.Leu135=
XR_001747785.2:n.955C>T
XR_947801.2:n.952-251C>T
NM_001382.4:c.921C>T MANE Select	NP_001373.2:p.Leu307=