Canonical Allele Identifier: CA382909729

Gene: DPAGT1

Linked Data

• MyVariant Identifiers: chr11:g.118968207C>A (hg19) ; chr11:g.119097497C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097497C>A , CM000673.2:g.119097497C>A	GRCh38
NC_000011.9:g.118968207C>A , CM000673.1:g.118968207C>A	GRCh37
NC_000011.8:g.118473417C>A	NCBI36
NG_008918.1:g.9579G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.1030G>T
ENST00000524658.2:n.1011G>T
ENST00000530052.2:n.2017G>T
ENST00000682191.1:n.1477G>T
ENST00000682192.1:n.1174G>T
ENST00000682232.1:c.*623-200G>T	ENSP00000507302.1:n.*623-200G>T
ENST00000682326.1:c.918-200G>T	ENSP00000508129.1:n.918-200G>T
ENST00000682404.1:n.2073G>T
ENST00000682517.1:n.2376G>T
ENST00000682652.1:n.2246G>T
ENST00000682665.1:n.1672G>T
ENST00000682691.1:n.1672G>T
ENST00000682791.1:c.885G>T	ENSP00000507312.1:p.Lys295Asn
ENST00000682811.1:c.*23G>T	ENSP00000508196.1:n.*23G>T
ENST00000682883.1:n.1032-200G>T
ENST00000682946.1:c.*54G>T	ENSP00000506856.1:n.*54G>T
ENST00000683143.1:c.*677G>T	ENSP00000507168.1:n.*677G>T
ENST00000683373.1:n.1477G>T
ENST00000683558.1:n.1477G>T
ENST00000683567.1:n.1081G>T
ENST00000683955.1:n.1728G>T
ENST00000684142.1:c.*647G>T	ENSP00000508008.1:n.*647G>T
ENST00000684252.1:n.1369G>T
ENST00000684255.1:c.*677G>T	ENSP00000507398.1:n.*677G>T
ENST00000684315.1:n.1705G>T
ENST00000684345.1:c.*950G>T	ENSP00000507163.1:n.*950G>T
ENST00000684499.1:c.*1077G>T	ENSP00000506800.1:n.*1077G>T
ENST00000684682.1:c.*703G>T	ENSP00000507326.1:n.*703G>T
ENST00000354202.9:c.972G>T MANE Select	ENSP00000346142.4:p.Lys324Asn
ENST00000636404.1:c.233-434G>T
ENST00000638850.1:c.476G>T
ENST00000639704.1:c.879G>T	ENSP00000491336.1:p.Lys293Asn
ENST00000640102.1:c.*625G>T	ENSP00000492027.1:n.*625G>T
ENST00000640747.1:c.*647G>T	ENSP00000492730.1:n.*647G>T
ENST00000354202.8:c.972G>T	ENSP00000346142.4:p.Lys324Asn
ENST00000392834.7:c.*677G>T	ENSP00000376579.3:n.*677G>T
ENST00000409993.6:c.972G>T	ENSP00000386597.2:p.Lys324Asn
ENST00000414373.5:c.*475-200G>T	ENSP00000402019.1:n.*475-200G>T
ENST00000442480.1:c.704G>T	ENSP00000406591.1:n.704G>T
ENST00000461999.1:n.1139G>T
ENST00000481084.5:n.1601G>T
ENST00000524658.1:n.277G>T
ENST00000525456.5:n.786G>T
NM_001382.3:c.972G>T	NP_001373.2:p.Lys324Asn
XM_005271422.2:c.972G>T	XP_005271479.1:p.Lys324Asn
XM_011542648.1:c.651G>T	XP_011540950.1:p.Lys217Asn
XR_947801.1:n.1165-200G>T
XM_005271422.3:c.972G>T	XP_005271479.1:p.Lys324Asn
XM_011542648.2:c.651G>T	XP_011540950.1:p.Lys217Asn
XM_017017293.2:c.651G>T	XP_016872782.1:p.Lys217Asn
XM_017017294.2:c.*54G>T	XP_016872783.1:n.*54G>T
XM_017017295.1:c.456G>T	XP_016872784.1:p.Lys152Asn
XR_001747785.2:n.1006G>T
XR_947801.2:n.952-200G>T
NM_001382.4:c.972G>T MANE Select	NP_001373.2:p.Lys324Asn