Canonical Allele Identifier: CA424402577

Gene: HNRNPU

Linked Data

• gnomAD v4: 1-244864110-G-T
• MyVariant Identifiers: chr1:g.245027412G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864110G>T , CM000663.2:g.244864110G>T	GRCh38
NC_000001.10:g.245027412G>T , CM000663.1:g.245027412G>T	GRCh37
NC_000001.9:g.243094035G>T	NCBI36
NG_042184.1:g.5416C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.198C>A	ENSP00000283179.10:p.Ser66=
ENST00000444376.7:c.198C>A	ENSP00000393151.2:p.Ser66=
ENST00000476241.2:n.383C>A
ENST00000638952.1:n.429C>A
ENST00000640218.2:c.198C>A MANE Select	ENSP00000491215.1:p.Ser66=
ENST00000640306.1:c.198C>A	ENSP00000491685.1:p.Ser66=
ENST00000649899.1:n.422C>A
ENST00000283179.13:c.198C>A	ENSP00000283179.9:p.Ser66=
ENST00000444376.6:c.198C>A	ENSP00000393151.2:p.Ser66=
ENST00000476241.1:n.382C>A
NM_004501.3:c.198C>A	NP_004492.2:p.Ser66=
NM_031844.2:c.198C>A	NP_114032.2:p.Ser66=
NM_031844.3:c.198C>A MANE Select	NP_114032.2:p.Ser66=