Canonical Allele Identifier: CA382914267

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118971026G>C (hg19) ; chr11:g.119100316G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119100316G>C , CM000673.2:g.119100316G>C	GRCh38
NC_000011.9:g.118971026G>C , CM000673.1:g.118971026G>C	GRCh37
NC_000011.8:g.118476236G>C	NCBI36
NG_008918.1:g.6760C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.765C>G
ENST00000530052.2:n.1331C>G
ENST00000682191.1:n.791C>G
ENST00000682192.1:n.791C>G
ENST00000682232.1:c.*294C>G	ENSP00000507302.1:n.*294C>G
ENST00000682326.1:c.589C>G	ENSP00000508129.1:p.Gln197Glu
ENST00000682404.1:n.1331C>G
ENST00000682517.1:n.1331C>G
ENST00000682652.1:n.1560C>G
ENST00000682665.1:n.986C>G
ENST00000682691.1:n.986C>G
ENST00000682791.1:c.502C>G	ENSP00000507312.1:p.Gln168Glu
ENST00000682811.1:c.589C>G	ENSP00000508196.1:p.Gln197Glu
ENST00000682883.1:n.892C>G
ENST00000682946.1:c.589C>G	ENSP00000506856.1:p.Gln197Glu
ENST00000683143.1:c.*294C>G	ENSP00000507168.1:n.*294C>G
ENST00000683373.1:n.791C>G
ENST00000683558.1:n.791C>G
ENST00000683567.1:n.816C>G
ENST00000683955.1:n.986C>G
ENST00000684142.1:c.*264C>G	ENSP00000508008.1:n.*264C>G
ENST00000684252.1:n.986C>G
ENST00000684255.1:c.*294C>G	ENSP00000507398.1:n.*294C>G
ENST00000684315.1:n.1322C>G
ENST00000684345.1:c.*264C>G	ENSP00000507163.1:n.*264C>G
ENST00000684499.1:c.*694C>G	ENSP00000506800.1:n.*694C>G
ENST00000684682.1:c.*17C>G	ENSP00000507326.1:n.*17C>G
ENST00000354202.9:c.589C>G MANE Select	ENSP00000346142.4:p.Gln197Glu
ENST00000636404.1:c.93C>G
ENST00000638850.1:c.93C>G
ENST00000639704.1:c.496C>G	ENSP00000491336.1:p.Gln166Glu
ENST00000640102.1:c.*242C>G	ENSP00000492027.1:n.*242C>G
ENST00000640747.1:c.*264C>G	ENSP00000492730.1:n.*264C>G
ENST00000354202.8:c.589C>G	ENSP00000346142.4:p.Gln197Glu
ENST00000392834.7:c.*294C>G	ENSP00000376579.3:n.*294C>G
ENST00000409993.6:c.589C>G	ENSP00000386597.2:p.Gln197Glu
ENST00000414373.5:c.*335C>G	ENSP00000402019.1:n.*335C>G
ENST00000442480.1:c.439C>G	ENSP00000406591.1:p.Gln147Glu
ENST00000461999.1:n.94C>G
ENST00000481084.5:n.1218C>G
ENST00000525456.5:n.592C>G
ENST00000530052.1:n.487C>G
ENST00000533687.1:n.601C>G
NM_001382.3:c.589C>G	NP_001373.2:p.Gln197Glu
XM_005271422.2:c.589C>G	XP_005271479.1:p.Gln197Glu
XM_011542648.1:c.268C>G	XP_011540950.1:p.Gln90Glu
XR_947801.1:n.1025C>G
XM_005271422.3:c.589C>G	XP_005271479.1:p.Gln197Glu
XM_011542648.2:c.268C>G	XP_011540950.1:p.Gln90Glu
XM_017017293.2:c.268C>G	XP_016872782.1:p.Gln90Glu
XM_017017294.2:c.589C>G	XP_016872783.1:p.Gln197Glu
XM_017017295.1:c.73C>G	XP_016872784.1:p.Gln25Glu
XR_001747785.2:n.812C>G
XR_947801.2:n.812C>G
NM_001382.4:c.589C>G MANE Select	NP_001373.2:p.Gln197Glu