Canonical Allele Identifier: CA382909652

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968199G>A (hg19) ; chr11:g.119097489G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097489G>A , CM000673.2:g.119097489G>A	GRCh38
NC_000011.9:g.118968199G>A , CM000673.1:g.118968199G>A	GRCh37
NC_000011.8:g.118473409G>A	NCBI36
NG_008918.1:g.9587C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1038C>T
ENST00000524658.2:n.1019C>T
ENST00000530052.2:n.2025C>T
ENST00000682191.1:n.1485C>T
ENST00000682192.1:n.1182C>T
ENST00000682232.1:c.*623-192C>T	ENSP00000507302.1:n.*623-192C>T
ENST00000682326.1:c.918-192C>T	ENSP00000508129.1:n.918-192C>T
ENST00000682404.1:n.2081C>T
ENST00000682517.1:n.2384C>T
ENST00000682652.1:n.2254C>T
ENST00000682665.1:n.1680C>T
ENST00000682691.1:n.1680C>T
ENST00000682791.1:c.893C>T	ENSP00000507312.1:p.Ser298Phe
ENST00000682811.1:c.*31C>T	ENSP00000508196.1:n.*31C>T
ENST00000682883.1:n.1032-192C>T
ENST00000682946.1:c.*62C>T	ENSP00000506856.1:n.*62C>T
ENST00000683143.1:c.*685C>T	ENSP00000507168.1:n.*685C>T
ENST00000683373.1:n.1485C>T
ENST00000683558.1:n.1485C>T
ENST00000683567.1:n.1089C>T
ENST00000683955.1:n.1736C>T
ENST00000684142.1:c.*655C>T	ENSP00000508008.1:n.*655C>T
ENST00000684252.1:n.1377C>T
ENST00000684255.1:c.*685C>T	ENSP00000507398.1:n.*685C>T
ENST00000684315.1:n.1713C>T
ENST00000684345.1:c.*958C>T	ENSP00000507163.1:n.*958C>T
ENST00000684499.1:c.*1085C>T	ENSP00000506800.1:n.*1085C>T
ENST00000684682.1:c.*711C>T	ENSP00000507326.1:n.*711C>T
ENST00000354202.9:c.980C>T MANE Select	ENSP00000346142.4:p.Ser327Phe
ENST00000636404.1:c.233-426C>T
ENST00000638850.1:c.484C>T
ENST00000639704.1:c.887C>T	ENSP00000491336.1:p.Ser296Phe
ENST00000640102.1:c.*633C>T	ENSP00000492027.1:n.*633C>T
ENST00000640747.1:c.*655C>T	ENSP00000492730.1:n.*655C>T
ENST00000354202.8:c.980C>T	ENSP00000346142.4:p.Ser327Phe
ENST00000392834.7:c.*685C>T	ENSP00000376579.3:n.*685C>T
ENST00000409993.6:c.980C>T	ENSP00000386597.2:p.Ser327Phe
ENST00000414373.5:c.*475-192C>T	ENSP00000402019.1:n.*475-192C>T
ENST00000442480.1:c.712C>T	ENSP00000406591.1:n.712C>T
ENST00000461999.1:n.1147C>T
ENST00000481084.5:n.1609C>T
ENST00000524658.1:n.285C>T
ENST00000525456.5:n.794C>T
NM_001382.3:c.980C>T	NP_001373.2:p.Ser327Phe
XM_005271422.2:c.980C>T	XP_005271479.1:p.Ser327Phe
XM_011542648.1:c.659C>T	XP_011540950.1:p.Ser220Phe
XR_947801.1:n.1165-192C>T
XM_005271422.3:c.980C>T	XP_005271479.1:p.Ser327Phe
XM_011542648.2:c.659C>T	XP_011540950.1:p.Ser220Phe
XM_017017293.2:c.659C>T	XP_016872782.1:p.Ser220Phe
XM_017017294.2:c.*62C>T	XP_016872783.1:n.*62C>T
XM_017017295.1:c.464C>T	XP_016872784.1:p.Ser155Phe
XR_001747785.2:n.1014C>T
XR_947801.2:n.952-192C>T
NM_001382.4:c.980C>T MANE Select	NP_001373.2:p.Ser327Phe