Canonical Allele Identifier: CA2616361162

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119097652-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097652A>C , CM000673.2:g.119097652A>C	GRCh38
NC_000011.9:g.118968362A>C , CM000673.1:g.118968362A>C	GRCh37
NC_000011.8:g.118473572A>C	NCBI36
NG_008918.1:g.9424T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-101T>G
ENST00000524658.2:n.957-101T>G
ENST00000530052.2:n.1862T>G
ENST00000682191.1:n.1322T>G
ENST00000682192.1:n.1120-101T>G
ENST00000682232.1:c.*622+203T>G	ENSP00000507302.1:n.*622+203T>G
ENST00000682326.1:c.917+203T>G	ENSP00000508129.1:n.917+203T>G
ENST00000682404.1:n.2019-101T>G
ENST00000682517.1:n.2221T>G
ENST00000682652.1:n.2091T>G
ENST00000682665.1:n.1517T>G
ENST00000682691.1:n.1517T>G
ENST00000682791.1:c.831-101T>G	ENSP00000507312.1:n.831-101T>G
ENST00000682811.1:c.800-101T>G	ENSP00000508196.1:n.800-101T>G
ENST00000682883.1:n.1032-355T>G
ENST00000682946.1:c.729-101T>G	ENSP00000506856.1:n.729-101T>G
ENST00000683143.1:c.*623-101T>G	ENSP00000507168.1:n.*623-101T>G
ENST00000683373.1:n.1322T>G
ENST00000683558.1:n.1322T>G
ENST00000683567.1:n.1027-101T>G
ENST00000683955.1:n.1674-101T>G
ENST00000684142.1:c.*593-101T>G	ENSP00000508008.1:n.*593-101T>G
ENST00000684252.1:n.1315-101T>G
ENST00000684255.1:c.*623-101T>G	ENSP00000507398.1:n.*623-101T>G
ENST00000684315.1:n.1651-101T>G
ENST00000684345.1:c.*795T>G	ENSP00000507163.1:n.*795T>G
ENST00000684499.1:c.*1023-101T>G	ENSP00000506800.1:n.*1023-101T>G
ENST00000684682.1:c.*548T>G	ENSP00000507326.1:n.*548T>G
ENST00000354202.9:c.918-101T>G MANE Select	ENSP00000346142.4:n.918-101T>G
ENST00000636404.1:c.233-589T>G
ENST00000638850.1:c.422-101T>G
ENST00000639704.1:c.825-101T>G	ENSP00000491336.1:n.825-101T>G
ENST00000640102.1:c.*571-101T>G	ENSP00000492027.1:n.*571-101T>G
ENST00000640747.1:c.*593-101T>G	ENSP00000492730.1:n.*593-101T>G
ENST00000354202.8:c.918-101T>G	ENSP00000346142.4:n.918-101T>G
ENST00000392834.7:c.*623-101T>G	ENSP00000376579.3:n.*623-101T>G
ENST00000409993.6:c.918-101T>G	ENSP00000386597.2:n.918-101T>G
ENST00000414373.5:c.*475-355T>G	ENSP00000402019.1:n.*475-355T>G
ENST00000442480.1:c.650-101T>G	ENSP00000406591.1:n.650-101T>G
ENST00000461999.1:n.984T>G
ENST00000481084.5:n.1547-101T>G
ENST00000524658.1:n.223-101T>G
ENST00000525456.5:n.732-101T>G
NM_001382.3:c.918-101T>G	NP_001373.2:n.918-101T>G
XM_005271422.2:c.918-101T>G	XP_005271479.1:n.918-101T>G
XM_011542648.1:c.597-101T>G	XP_011540950.1:n.597-101T>G
XR_947801.1:n.1165-355T>G
XM_005271422.3:c.918-101T>G	XP_005271479.1:n.918-101T>G
XM_011542648.2:c.597-101T>G	XP_011540950.1:n.597-101T>G
XM_017017293.2:c.597-101T>G	XP_016872782.1:n.597-101T>G
XM_017017294.2:c.729-101T>G	XP_016872783.1:n.729-101T>G
XM_017017295.1:c.402-101T>G	XP_016872784.1:n.402-101T>G
XR_001747785.2:n.952-101T>G
XR_947801.2:n.952-355T>G
NM_001382.4:c.918-101T>G MANE Select	NP_001373.2:n.918-101T>G