Canonical Allele Identifier: CA424402692

Gene: HNRNPU

Linked Data

• gnomAD v4: 1-244863849-G-T
• MyVariant Identifiers: chr1:g.245027151G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863849G>T , CM000663.2:g.244863849G>T	GRCh38
NC_000001.10:g.245027151G>T , CM000663.1:g.245027151G>T	GRCh37
NC_000001.9:g.243093774G>T	NCBI36
NG_042184.1:g.5677C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.137C>A
ENST00000283179.14:c.459C>A	ENSP00000283179.10:p.Gly153=
ENST00000444376.7:c.459C>A	ENSP00000393151.2:p.Gly153=
ENST00000476241.2:n.644C>A
ENST00000638475.1:c.243C>A	ENSP00000491305.1:p.Gly81=
ENST00000638952.1:n.690C>A
ENST00000640218.2:c.459C>A MANE Select	ENSP00000491215.1:p.Gly153=
ENST00000640306.1:c.459C>A	ENSP00000491685.1:p.Gly153=
ENST00000640440.1:c.159C>A	ENSP00000491263.1:p.Gly53=
ENST00000649899.1:n.683C>A
ENST00000283179.13:c.459C>A	ENSP00000283179.9:p.Gly153=
ENST00000444376.6:c.459C>A	ENSP00000393151.2:p.Gly153=
ENST00000476241.1:n.643C>A
NM_004501.3:c.459C>A	NP_004492.2:p.Gly153=
NM_031844.2:c.459C>A	NP_114032.2:p.Gly153=
NM_031844.3:c.459C>A MANE Select	NP_114032.2:p.Gly153=