Canonical Allele Identifier: CA602578242

Gene: DPAGT1

Linked Data

• dbSNP Id: rs1302541541
• gnomAD v2: 11-118968352-C-A
• gnomAD v4: 11-119097642-C-A
• MyVariant Identifiers: chr11:g.118968352C>A (hg19) ; chr11:g.119097642C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097642C>A , CM000673.2:g.119097642C>A	GRCh38
NC_000011.9:g.118968352C>A , CM000673.1:g.118968352C>A	GRCh37
NC_000011.8:g.118473562C>A	NCBI36
NG_008918.1:g.9434G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-91G>T
ENST00000524658.2:n.957-91G>T
ENST00000530052.2:n.1872G>T
ENST00000682191.1:n.1332G>T
ENST00000682192.1:n.1120-91G>T
ENST00000682232.1:c.*622+213G>T	ENSP00000507302.1:n.*622+213G>T
ENST00000682326.1:c.917+213G>T	ENSP00000508129.1:n.917+213G>T
ENST00000682404.1:n.2019-91G>T
ENST00000682517.1:n.2231G>T
ENST00000682652.1:n.2101G>T
ENST00000682665.1:n.1527G>T
ENST00000682691.1:n.1527G>T
ENST00000682791.1:c.831-91G>T	ENSP00000507312.1:n.831-91G>T
ENST00000682811.1:c.800-91G>T	ENSP00000508196.1:n.800-91G>T
ENST00000682883.1:n.1032-345G>T
ENST00000682946.1:c.729-91G>T	ENSP00000506856.1:n.729-91G>T
ENST00000683143.1:c.*623-91G>T	ENSP00000507168.1:n.*623-91G>T
ENST00000683373.1:n.1332G>T
ENST00000683558.1:n.1332G>T
ENST00000683567.1:n.1027-91G>T
ENST00000683955.1:n.1674-91G>T
ENST00000684142.1:c.*593-91G>T	ENSP00000508008.1:n.*593-91G>T
ENST00000684252.1:n.1315-91G>T
ENST00000684255.1:c.*623-91G>T	ENSP00000507398.1:n.*623-91G>T
ENST00000684315.1:n.1651-91G>T
ENST00000684345.1:c.*805G>T	ENSP00000507163.1:n.*805G>T
ENST00000684499.1:c.*1023-91G>T	ENSP00000506800.1:n.*1023-91G>T
ENST00000684682.1:c.*558G>T	ENSP00000507326.1:n.*558G>T
ENST00000354202.9:c.918-91G>T MANE Select	ENSP00000346142.4:n.918-91G>T
ENST00000636404.1:c.233-579G>T
ENST00000638850.1:c.422-91G>T
ENST00000639704.1:c.825-91G>T	ENSP00000491336.1:n.825-91G>T
ENST00000640102.1:c.*571-91G>T	ENSP00000492027.1:n.*571-91G>T
ENST00000640747.1:c.*593-91G>T	ENSP00000492730.1:n.*593-91G>T
ENST00000354202.8:c.918-91G>T	ENSP00000346142.4:n.918-91G>T
ENST00000392834.7:c.*623-91G>T	ENSP00000376579.3:n.*623-91G>T
ENST00000409993.6:c.918-91G>T	ENSP00000386597.2:n.918-91G>T
ENST00000414373.5:c.*475-345G>T	ENSP00000402019.1:n.*475-345G>T
ENST00000442480.1:c.650-91G>T	ENSP00000406591.1:n.650-91G>T
ENST00000461999.1:n.994G>T
ENST00000481084.5:n.1547-91G>T
ENST00000524658.1:n.223-91G>T
ENST00000525456.5:n.732-91G>T
NM_001382.3:c.918-91G>T	NP_001373.2:n.918-91G>T
XM_005271422.2:c.918-91G>T	XP_005271479.1:n.918-91G>T
XM_011542648.1:c.597-91G>T	XP_011540950.1:n.597-91G>T
XR_947801.1:n.1165-345G>T
XM_005271422.3:c.918-91G>T	XP_005271479.1:n.918-91G>T
XM_011542648.2:c.597-91G>T	XP_011540950.1:n.597-91G>T
XM_017017293.2:c.597-91G>T	XP_016872782.1:n.597-91G>T
XM_017017294.2:c.729-91G>T	XP_016872783.1:n.729-91G>T
XM_017017295.1:c.402-91G>T	XP_016872784.1:n.402-91G>T
XR_001747785.2:n.952-91G>T
XR_947801.2:n.952-345G>T
NM_001382.4:c.918-91G>T MANE Select	NP_001373.2:n.918-91G>T