Canonical Allele Identifier: CA345497562

Gene: HNRNPU

Linked Data

• dbSNP Id: rs1302622066
• gnomAD v2: 1-245027365-C-T
• gnomAD v4: 1-244864063-C-T
• MyVariant Identifiers: chr1:g.245027365C>T (hg19) ; chr1:g.244864063C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864063C>T , CM000663.2:g.244864063C>T	GRCh38
NC_000001.10:g.245027365C>T , CM000663.1:g.245027365C>T	GRCh37
NC_000001.9:g.243093988C>T	NCBI36
NG_042184.1:g.5463G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.245G>A	ENSP00000283179.10:p.Gly82Asp
ENST00000444376.7:c.245G>A	ENSP00000393151.2:p.Gly82Asp
ENST00000476241.2:n.430G>A
ENST00000638475.1:c.29G>A	ENSP00000491305.1:p.Gly10Asp
ENST00000638952.1:n.476G>A
ENST00000640218.2:c.245G>A MANE Select	ENSP00000491215.1:p.Gly82Asp
ENST00000640306.1:c.245G>A	ENSP00000491685.1:p.Gly82Asp
ENST00000649899.1:n.469G>A
ENST00000283179.13:c.245G>A	ENSP00000283179.9:p.Gly82Asp
ENST00000444376.6:c.245G>A	ENSP00000393151.2:p.Gly82Asp
ENST00000476241.1:n.429G>A
NM_004501.3:c.245G>A	NP_004492.2:p.Gly82Asp
NM_031844.2:c.245G>A	NP_114032.2:p.Gly82Asp
NM_031844.3:c.245G>A MANE Select	NP_114032.2:p.Gly82Asp