Canonical Allele Identifier: CA345497176

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027198A>C (hg19) ; chr1:g.244863896A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863896A>C , CM000663.2:g.244863896A>C	GRCh38
NC_000001.10:g.245027198A>C , CM000663.1:g.245027198A>C	GRCh37
NC_000001.9:g.243093821A>C	NCBI36
NG_042184.1:g.5630T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.90T>G
ENST00000283179.14:c.412T>G	ENSP00000283179.10:p.Phe138Val
ENST00000444376.7:c.412T>G	ENSP00000393151.2:p.Phe138Val
ENST00000476241.2:n.597T>G
ENST00000638475.1:c.196T>G	ENSP00000491305.1:p.Phe66Val
ENST00000638952.1:n.643T>G
ENST00000640218.2:c.412T>G MANE Select	ENSP00000491215.1:p.Phe138Val
ENST00000640306.1:c.412T>G	ENSP00000491685.1:p.Phe138Val
ENST00000640440.1:c.112T>G	ENSP00000491263.1:p.Phe38Val
ENST00000649899.1:n.636T>G
ENST00000283179.13:c.412T>G	ENSP00000283179.9:p.Phe138Val
ENST00000444376.6:c.412T>G	ENSP00000393151.2:p.Phe138Val
ENST00000476241.1:n.596T>G
NM_004501.3:c.412T>G	NP_004492.2:p.Phe138Val
NM_031844.2:c.412T>G	NP_114032.2:p.Phe138Val
NM_031844.3:c.412T>G MANE Select	NP_114032.2:p.Phe138Val