Canonical Allele Identifier: CA345497029

Gene: HNRNPU

Linked Data

• ClinVar Variation Id: 951324
• ClinVar RCV Id: RCV002562579
• dbSNP Id: rs1680926034
• gnomAD v4: 1-244863853-G-A
• MyVariant Identifiers: chr1:g.245027155G>A (hg19) ; chr1:g.244863853G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863853G>A , CM000663.2:g.244863853G>A	GRCh38
NC_000001.10:g.245027155G>A , CM000663.1:g.245027155G>A	GRCh37
NC_000001.9:g.243093778G>A	NCBI36
NG_042184.1:g.5673C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.133C>T
ENST00000283179.14:c.455C>T	ENSP00000283179.10:p.Ala152Val
ENST00000444376.7:c.455C>T	ENSP00000393151.2:p.Ala152Val
ENST00000476241.2:n.640C>T
ENST00000638475.1:c.239C>T	ENSP00000491305.1:p.Ala80Val
ENST00000638952.1:n.686C>T
ENST00000640218.2:c.455C>T MANE Select	ENSP00000491215.1:p.Ala152Val
ENST00000640306.1:c.455C>T	ENSP00000491685.1:p.Ala152Val
ENST00000640440.1:c.155C>T	ENSP00000491263.1:p.Ala52Val
ENST00000649899.1:n.679C>T
ENST00000283179.13:c.455C>T	ENSP00000283179.9:p.Ala152Val
ENST00000444376.6:c.455C>T	ENSP00000393151.2:p.Ala152Val
ENST00000476241.1:n.639C>T
NM_004501.3:c.455C>T	NP_004492.2:p.Ala152Val
NM_031844.2:c.455C>T	NP_114032.2:p.Ala152Val
NM_031844.3:c.455C>T MANE Select	NP_114032.2:p.Ala152Val