Canonical Allele Identifier: CA345497080

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027165C>T (hg19) ; chr1:g.244863863C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863863C>T , CM000663.2:g.244863863C>T	GRCh38
NC_000001.10:g.245027165C>T , CM000663.1:g.245027165C>T	GRCh37
NC_000001.9:g.243093788C>T	NCBI36
NG_042184.1:g.5663G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000704074.1:c.123G>A
ENST00000283179.14:c.445G>A	ENSP00000283179.10:p.Glu149Lys
ENST00000444376.7:c.445G>A	ENSP00000393151.2:p.Glu149Lys
ENST00000476241.2:n.630G>A
ENST00000638475.1:c.229G>A	ENSP00000491305.1:p.Glu77Lys
ENST00000638952.1:n.676G>A
ENST00000640218.2:c.445G>A MANE Select	ENSP00000491215.1:p.Glu149Lys
ENST00000640306.1:c.445G>A	ENSP00000491685.1:p.Glu149Lys
ENST00000640440.1:c.145G>A	ENSP00000491263.1:p.Glu49Lys
ENST00000649899.1:n.669G>A
ENST00000283179.13:c.445G>A	ENSP00000283179.9:p.Glu149Lys
ENST00000444376.6:c.445G>A	ENSP00000393151.2:p.Glu149Lys
ENST00000476241.1:n.629G>A
NM_004501.3:c.445G>A	NP_004492.2:p.Glu149Lys
NM_031844.2:c.445G>A	NP_114032.2:p.Glu149Lys
NM_031844.3:c.445G>A MANE Select	NP_114032.2:p.Glu149Lys