Canonical Allele Identifier: CA345497181

Gene: HNRNPU

Linked Data

• gnomAD v4: 1-244863898-C-T
• MyVariant Identifiers: chr1:g.245027200C>T (hg19) ; chr1:g.244863898C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863898C>T , CM000663.2:g.244863898C>T	GRCh38
NC_000001.10:g.245027200C>T , CM000663.1:g.245027200C>T	GRCh37
NC_000001.9:g.243093823C>T	NCBI36
NG_042184.1:g.5628G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.88G>A
ENST00000283179.14:c.410G>A	ENSP00000283179.10:p.Gly137Asp
ENST00000444376.7:c.410G>A	ENSP00000393151.2:p.Gly137Asp
ENST00000476241.2:n.595G>A
ENST00000638475.1:c.194G>A	ENSP00000491305.1:p.Gly65Asp
ENST00000638952.1:n.641G>A
ENST00000640218.2:c.410G>A MANE Select	ENSP00000491215.1:p.Gly137Asp
ENST00000640306.1:c.410G>A	ENSP00000491685.1:p.Gly137Asp
ENST00000640440.1:c.110G>A	ENSP00000491263.1:p.Gly37Asp
ENST00000649899.1:n.634G>A
ENST00000283179.13:c.410G>A	ENSP00000283179.9:p.Gly137Asp
ENST00000444376.6:c.410G>A	ENSP00000393151.2:p.Gly137Asp
ENST00000476241.1:n.594G>A
NM_004501.3:c.410G>A	NP_004492.2:p.Gly137Asp
NM_031844.2:c.410G>A	NP_114032.2:p.Gly137Asp
NM_031844.3:c.410G>A MANE Select	NP_114032.2:p.Gly137Asp