Canonical Allele Identifier: CA424402502

Gene: HNRNPU

Linked Data

• dbSNP Id: rs1317989761
• gnomAD v2: 1-245026977-T-C
• gnomAD v4: 1-244863675-T-C
• MyVariant Identifiers: chr1:g.245026977T>C (hg19) ; chr1:g.244863675T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863675T>C , CM000663.2:g.244863675T>C	GRCh38
NC_000001.10:g.245026977T>C , CM000663.1:g.245026977T>C	GRCh37
NC_000001.9:g.243093600T>C	NCBI36
NG_042184.1:g.5851A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.311A>G
ENST00000283179.14:c.633A>G	ENSP00000283179.10:p.Gly211=
ENST00000444376.7:c.633A>G	ENSP00000393151.2:p.Gly211=
ENST00000476241.2:n.818A>G
ENST00000638475.1:c.417A>G	ENSP00000491305.1:p.Gly139=
ENST00000638952.1:n.864A>G
ENST00000640218.2:c.633A>G MANE Select	ENSP00000491215.1:p.Gly211=
ENST00000640306.1:c.633A>G	ENSP00000491685.1:p.Gly211=
ENST00000640440.1:c.333A>G	ENSP00000491263.1:p.Gly111=
ENST00000649899.1:n.857A>G
ENST00000283179.13:c.633A>G	ENSP00000283179.9:p.Gly211=
ENST00000444376.6:c.633A>G	ENSP00000393151.2:p.Gly211=
ENST00000476241.1:n.817A>G
NM_004501.3:c.633A>G	NP_004492.2:p.Gly211=
NM_031844.2:c.633A>G	NP_114032.2:p.Gly211=
NM_031844.3:c.633A>G MANE Select	NP_114032.2:p.Gly211=