Canonical Allele Identifier: CA602578241

Gene: DPAGT1

Linked Data

• dbSNP Id: rs1346793915
• gnomAD v2: 11-118968325-TA-T
• gnomAD v3: 11-119097615-TA-T
• gnomAD v4: 11-119097615-TA-T
• MyVariant Identifiers: chr11:g.118968326del (hg19) ; chr11:g.119097616del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097616del , CM000673.2:g.119097616del	GRCh38
NC_000011.9:g.118968326del , CM000673.1:g.118968326del	GRCh37
NC_000011.8:g.118473536del	NCBI36
NG_008918.1:g.9460del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-65del
ENST00000524658.2:n.957-65del
ENST00000530052.2:n.1898del
ENST00000682191.1:n.1358del
ENST00000682192.1:n.1120-65del
ENST00000682232.1:c.*622+239del	ENSP00000507302.1:n.*622+239del
ENST00000682326.1:c.917+239del	ENSP00000508129.1:n.917+239del
ENST00000682404.1:n.2019-65del
ENST00000682517.1:n.2257del
ENST00000682652.1:n.2127del
ENST00000682665.1:n.1553del
ENST00000682691.1:n.1553del
ENST00000682791.1:c.831-65del	ENSP00000507312.1:n.831-65del
ENST00000682811.1:c.800-65del	ENSP00000508196.1:n.800-65del
ENST00000682883.1:n.1032-319del
ENST00000682946.1:c.729-65del	ENSP00000506856.1:n.729-65del
ENST00000683143.1:c.*623-65del	ENSP00000507168.1:n.*623-65del
ENST00000683373.1:n.1358del
ENST00000683558.1:n.1358del
ENST00000683567.1:n.1027-65del
ENST00000683955.1:n.1674-65del
ENST00000684142.1:c.*593-65del	ENSP00000508008.1:n.*593-65del
ENST00000684252.1:n.1315-65del
ENST00000684255.1:c.*623-65del	ENSP00000507398.1:n.*623-65del
ENST00000684315.1:n.1651-65del
ENST00000684345.1:c.*831del	ENSP00000507163.1:n.*831del
ENST00000684499.1:c.*1023-65del	ENSP00000506800.1:n.*1023-65del
ENST00000684682.1:c.*584del	ENSP00000507326.1:n.*584del
ENST00000354202.9:c.918-65del MANE Select	ENSP00000346142.4:n.918-65del
ENST00000636404.1:c.233-553del
ENST00000638850.1:c.422-65del
ENST00000639704.1:c.825-65del	ENSP00000491336.1:n.825-65del
ENST00000640102.1:c.*571-65del	ENSP00000492027.1:n.*571-65del
ENST00000640747.1:c.*593-65del	ENSP00000492730.1:n.*593-65del
ENST00000354202.8:c.918-65del	ENSP00000346142.4:n.918-65del
ENST00000392834.7:c.*623-65del	ENSP00000376579.3:n.*623-65del
ENST00000409993.6:c.918-65del	ENSP00000386597.2:n.918-65del
ENST00000414373.5:c.*475-319del	ENSP00000402019.1:n.*475-319del
ENST00000442480.1:c.650-65del	ENSP00000406591.1:n.650-65del
ENST00000461999.1:n.1020del
ENST00000481084.5:n.1547-65del
ENST00000524658.1:n.223-65del
ENST00000525456.5:n.732-65del
NM_001382.3:c.918-65del	NP_001373.2:n.918-65del
XM_005271422.2:c.918-65del	XP_005271479.1:n.918-65del
XM_011542648.1:c.597-65del	XP_011540950.1:n.597-65del
XR_947801.1:n.1165-319del
XM_005271422.3:c.918-65del	XP_005271479.1:n.918-65del
XM_011542648.2:c.597-65del	XP_011540950.1:n.597-65del
XM_017017293.2:c.597-65del	XP_016872782.1:n.597-65del
XM_017017294.2:c.729-65del	XP_016872783.1:n.729-65del
XM_017017295.1:c.402-65del	XP_016872784.1:n.402-65del
XR_001747785.2:n.952-65del
XR_947801.2:n.952-319del
NM_001382.4:c.918-65del MANE Select	NP_001373.2:n.918-65del