Canonical Allele Identifier: CA424402495

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027367G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864065G>C , CM000663.2:g.244864065G>C	GRCh38
NC_000001.10:g.245027367G>C , CM000663.1:g.245027367G>C	GRCh37
NC_000001.9:g.243093990G>C	NCBI36
NG_042184.1:g.5461C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.243C>G	ENSP00000283179.10:p.Gly81=
ENST00000444376.7:c.243C>G	ENSP00000393151.2:p.Gly81=
ENST00000476241.2:n.428C>G
ENST00000638475.1:c.27C>G	ENSP00000491305.1:p.Gly9=
ENST00000638952.1:n.474C>G
ENST00000640218.2:c.243C>G MANE Select	ENSP00000491215.1:p.Gly81=
ENST00000640306.1:c.243C>G	ENSP00000491685.1:p.Gly81=
ENST00000649899.1:n.467C>G
ENST00000283179.13:c.243C>G	ENSP00000283179.9:p.Gly81=
ENST00000444376.6:c.243C>G	ENSP00000393151.2:p.Gly81=
ENST00000476241.1:n.427C>G
NM_004501.3:c.243C>G	NP_004492.2:p.Gly81=
NM_031844.2:c.243C>G	NP_114032.2:p.Gly81=
NM_031844.3:c.243C>G MANE Select	NP_114032.2:p.Gly81=