Canonical Allele Identifier: CA345496809

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027107G>T (hg19) ; chr1:g.244863805G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863805G>T , CM000663.2:g.244863805G>T	GRCh38
NC_000001.10:g.245027107G>T , CM000663.1:g.245027107G>T	GRCh37
NC_000001.9:g.243093730G>T	NCBI36
NG_042184.1:g.5721C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.181C>A
ENST00000283179.14:c.503C>A	ENSP00000283179.10:p.Thr168Lys
ENST00000444376.7:c.503C>A	ENSP00000393151.2:p.Thr168Lys
ENST00000476241.2:n.688C>A
ENST00000638475.1:c.287C>A	ENSP00000491305.1:p.Thr96Lys
ENST00000638952.1:n.734C>A
ENST00000640218.2:c.503C>A MANE Select	ENSP00000491215.1:p.Thr168Lys
ENST00000640306.1:c.503C>A	ENSP00000491685.1:p.Thr168Lys
ENST00000640440.1:c.203C>A	ENSP00000491263.1:p.Thr68Lys
ENST00000649899.1:n.727C>A
ENST00000283179.13:c.503C>A	ENSP00000283179.9:p.Thr168Lys
ENST00000444376.6:c.503C>A	ENSP00000393151.2:p.Thr168Lys
ENST00000476241.1:n.687C>A
NM_004501.3:c.503C>A	NP_004492.2:p.Thr168Lys
NM_031844.2:c.503C>A	NP_114032.2:p.Thr168Lys
NM_031844.3:c.503C>A MANE Select	NP_114032.2:p.Thr168Lys