Canonical Allele Identifier: CA2651343593

Gene: HNRNPU

Linked Data

• gnomAD v4: 1-244863988-C-CCTA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863989_244863991dup , CM000663.2:g.244863989_244863991dup	GRCh38
NC_000001.10:g.245027291_245027293dup , CM000663.1:g.245027291_245027293dup	GRCh37
NC_000001.9:g.243093914_243093916dup	NCBI36
NG_042184.1:g.5535_5537dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.317_319dup	ENSP00000283179.10:p.Leu106_Gly107insVal
ENST00000444376.7:c.317_319dup	ENSP00000393151.2:p.Leu106_Gly107insVal
ENST00000476241.2:n.502_504dup
ENST00000638475.1:c.101_103dup	ENSP00000491305.1:p.Leu34_Gly35insVal
ENST00000638952.1:n.548_550dup
ENST00000640218.2:c.317_319dup MANE Select	ENSP00000491215.1:p.Leu106_Gly107insVal
ENST00000640306.1:c.317_319dup	ENSP00000491685.1:p.Leu106_Gly107insVal
ENST00000640440.1:c.17_19dup	ENSP00000491263.1:p.Leu6_Gly7insVal
ENST00000649899.1:n.541_543dup
ENST00000283179.13:c.317_319dup	ENSP00000283179.9:p.Leu106_Gly107insVal
ENST00000444376.6:c.317_319dup	ENSP00000393151.2:p.Leu106_Gly107insVal
ENST00000476241.1:n.501_503dup
NM_004501.3:c.317_319dup	NP_004492.2:p.Leu106_Gly107insVal
NM_031844.2:c.317_319dup	NP_114032.2:p.Leu106_Gly107insVal
NM_031844.3:c.317_319dup MANE Select	NP_114032.2:p.Leu106_Gly107insVal