Canonical Allele Identifier: CA424402648

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027106C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863804C>G , CM000663.2:g.244863804C>G	GRCh38
NC_000001.10:g.245027106C>G , CM000663.1:g.245027106C>G	GRCh37
NC_000001.9:g.243093729C>G	NCBI36
NG_042184.1:g.5722G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.182G>C
ENST00000283179.14:c.504G>C	ENSP00000283179.10:p.Thr168=
ENST00000444376.7:c.504G>C	ENSP00000393151.2:p.Thr168=
ENST00000476241.2:n.689G>C
ENST00000638475.1:c.288G>C	ENSP00000491305.1:p.Thr96=
ENST00000638952.1:n.735G>C
ENST00000640218.2:c.504G>C MANE Select	ENSP00000491215.1:p.Thr168=
ENST00000640306.1:c.504G>C	ENSP00000491685.1:p.Thr168=
ENST00000640440.1:c.204G>C	ENSP00000491263.1:p.Thr68=
ENST00000649899.1:n.728G>C
ENST00000283179.13:c.504G>C	ENSP00000283179.9:p.Thr168=
ENST00000444376.6:c.504G>C	ENSP00000393151.2:p.Thr168=
ENST00000476241.1:n.688G>C
NM_004501.3:c.504G>C	NP_004492.2:p.Thr168=
NM_031844.2:c.504G>C	NP_114032.2:p.Thr168=
NM_031844.3:c.504G>C MANE Select	NP_114032.2:p.Thr168=