Canonical Allele Identifier: CA382914163

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118971017C>A (hg19) ; chr11:g.119100307C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100307C>A , CM000673.2:g.119100307C>A	GRCh38
NC_000011.9:g.118971017C>A , CM000673.1:g.118971017C>A	GRCh37
NC_000011.8:g.118476227C>A	NCBI36
NG_008918.1:g.6769G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000445653.6:n.774G>T
ENST00000530052.2:n.1340G>T
ENST00000682191.1:n.800G>T
ENST00000682192.1:n.800G>T
ENST00000682232.1:c.*303G>T	ENSP00000507302.1:n.*303G>T
ENST00000682326.1:c.598G>T	ENSP00000508129.1:p.Val200Phe
ENST00000682404.1:n.1340G>T
ENST00000682517.1:n.1340G>T
ENST00000682652.1:n.1569G>T
ENST00000682665.1:n.995G>T
ENST00000682691.1:n.995G>T
ENST00000682791.1:c.511G>T	ENSP00000507312.1:p.Val171Phe
ENST00000682811.1:c.598G>T	ENSP00000508196.1:p.Val200Phe
ENST00000682883.1:n.901G>T
ENST00000682946.1:c.598G>T	ENSP00000506856.1:p.Val200Phe
ENST00000683143.1:c.*303G>T	ENSP00000507168.1:n.*303G>T
ENST00000683373.1:n.800G>T
ENST00000683558.1:n.800G>T
ENST00000683567.1:n.825G>T
ENST00000683955.1:n.995G>T
ENST00000684142.1:c.*273G>T	ENSP00000508008.1:n.*273G>T
ENST00000684252.1:n.995G>T
ENST00000684255.1:c.*303G>T	ENSP00000507398.1:n.*303G>T
ENST00000684315.1:n.1331G>T
ENST00000684345.1:c.*273G>T	ENSP00000507163.1:n.*273G>T
ENST00000684499.1:c.*703G>T	ENSP00000506800.1:n.*703G>T
ENST00000684682.1:c.*26G>T	ENSP00000507326.1:n.*26G>T
ENST00000354202.9:c.598G>T MANE Select	ENSP00000346142.4:p.Val200Phe
ENST00000636404.1:c.102G>T
ENST00000638850.1:c.102G>T
ENST00000639704.1:c.505G>T	ENSP00000491336.1:p.Val169Phe
ENST00000640102.1:c.*251G>T	ENSP00000492027.1:n.*251G>T
ENST00000640747.1:c.*273G>T	ENSP00000492730.1:n.*273G>T
ENST00000354202.8:c.598G>T	ENSP00000346142.4:p.Val200Phe
ENST00000392834.7:c.*303G>T	ENSP00000376579.3:n.*303G>T
ENST00000409993.6:c.598G>T	ENSP00000386597.2:p.Val200Phe
ENST00000414373.5:c.*344G>T	ENSP00000402019.1:n.*344G>T
ENST00000442480.1:c.448G>T	ENSP00000406591.1:p.Val150Phe
ENST00000461999.1:n.103G>T
ENST00000481084.5:n.1227G>T
ENST00000525456.5:n.601G>T
ENST00000530052.1:n.496G>T
ENST00000533687.1:n.610G>T
NM_001382.3:c.598G>T	NP_001373.2:p.Val200Phe
XM_005271422.2:c.598G>T	XP_005271479.1:p.Val200Phe
XM_011542648.1:c.277G>T	XP_011540950.1:p.Val93Phe
XR_947801.1:n.1034G>T
XM_005271422.3:c.598G>T	XP_005271479.1:p.Val200Phe
XM_011542648.2:c.277G>T	XP_011540950.1:p.Val93Phe
XM_017017293.2:c.277G>T	XP_016872782.1:p.Val93Phe
XM_017017294.2:c.598G>T	XP_016872783.1:p.Val200Phe
XM_017017295.1:c.82G>T	XP_016872784.1:p.Val28Phe
XR_001747785.2:n.821G>T
XR_947801.2:n.821G>T
NM_001382.4:c.598G>T MANE Select	NP_001373.2:p.Val200Phe