Canonical Allele Identifier: CA2616361147

Gene: DPAGT1

Linked Data

• gnomAD v4: 11-119097639-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119097641dup , CM000673.2:g.119097641dup	GRCh38
NC_000011.9:g.118968351dup , CM000673.1:g.118968351dup	GRCh37
NC_000011.8:g.118473561dup	NCBI36
NG_008918.1:g.9436dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000445653.6:n.976-89dup
ENST00000524658.2:n.957-89dup
ENST00000530052.2:n.1874dup
ENST00000682191.1:n.1334dup
ENST00000682192.1:n.1120-89dup
ENST00000682232.1:c.*622+215dup	ENSP00000507302.1:n.*622+215dup
ENST00000682326.1:c.917+215dup	ENSP00000508129.1:n.917+215dup
ENST00000682404.1:n.2019-89dup
ENST00000682517.1:n.2233dup
ENST00000682652.1:n.2103dup
ENST00000682665.1:n.1529dup
ENST00000682691.1:n.1529dup
ENST00000682791.1:c.831-89dup	ENSP00000507312.1:n.831-89dup
ENST00000682811.1:c.800-89dup	ENSP00000508196.1:n.800-89dup
ENST00000682883.1:n.1032-343dup
ENST00000682946.1:c.729-89dup	ENSP00000506856.1:n.729-89dup
ENST00000683143.1:c.*623-89dup	ENSP00000507168.1:n.*623-89dup
ENST00000683373.1:n.1334dup
ENST00000683558.1:n.1334dup
ENST00000683567.1:n.1027-89dup
ENST00000683955.1:n.1674-89dup
ENST00000684142.1:c.*593-89dup	ENSP00000508008.1:n.*593-89dup
ENST00000684252.1:n.1315-89dup
ENST00000684255.1:c.*623-89dup	ENSP00000507398.1:n.*623-89dup
ENST00000684315.1:n.1651-89dup
ENST00000684345.1:c.*807dup	ENSP00000507163.1:n.*807dup
ENST00000684499.1:c.*1023-89dup	ENSP00000506800.1:n.*1023-89dup
ENST00000684682.1:c.*560dup	ENSP00000507326.1:n.*560dup
ENST00000354202.9:c.918-89dup MANE Select	ENSP00000346142.4:n.918-89dup
ENST00000636404.1:c.233-577dup
ENST00000638850.1:c.422-89dup
ENST00000639704.1:c.825-89dup	ENSP00000491336.1:n.825-89dup
ENST00000640102.1:c.*571-89dup	ENSP00000492027.1:n.*571-89dup
ENST00000640747.1:c.*593-89dup	ENSP00000492730.1:n.*593-89dup
ENST00000354202.8:c.918-89dup	ENSP00000346142.4:n.918-89dup
ENST00000392834.7:c.*623-89dup	ENSP00000376579.3:n.*623-89dup
ENST00000409993.6:c.918-89dup	ENSP00000386597.2:n.918-89dup
ENST00000414373.5:c.*475-343dup	ENSP00000402019.1:n.*475-343dup
ENST00000442480.1:c.650-89dup	ENSP00000406591.1:n.650-89dup
ENST00000461999.1:n.996dup
ENST00000481084.5:n.1547-89dup
ENST00000524658.1:n.223-89dup
ENST00000525456.5:n.732-89dup
NM_001382.3:c.918-89dup	NP_001373.2:n.918-89dup
XM_005271422.2:c.918-89dup	XP_005271479.1:n.918-89dup
XM_011542648.1:c.597-89dup	XP_011540950.1:n.597-89dup
XR_947801.1:n.1165-343dup
XM_005271422.3:c.918-89dup	XP_005271479.1:n.918-89dup
XM_011542648.2:c.597-89dup	XP_011540950.1:n.597-89dup
XM_017017293.2:c.597-89dup	XP_016872782.1:n.597-89dup
XM_017017294.2:c.729-89dup	XP_016872783.1:n.729-89dup
XM_017017295.1:c.402-89dup	XP_016872784.1:n.402-89dup
XR_001747785.2:n.952-89dup
XR_947801.2:n.952-343dup
NM_001382.4:c.918-89dup MANE Select	NP_001373.2:n.918-89dup