Canonical Allele Identifier: CA424402468

Gene: HNRNPU

Linked Data

• gnomAD v4: 1-244863642-G-T
• MyVariant Identifiers: chr1:g.245026944G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863642G>T , CM000663.2:g.244863642G>T	GRCh38
NC_000001.10:g.245026944G>T , CM000663.1:g.245026944G>T	GRCh37
NC_000001.9:g.243093567G>T	NCBI36
NG_042184.1:g.5884C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.312+32C>A
ENST00000283179.14:c.634+32C>A	ENSP00000283179.10:n.634+32C>A
ENST00000444376.7:c.634+32C>A	ENSP00000393151.2:n.634+32C>A
ENST00000476241.2:n.819+32C>A
ENST00000638475.1:c.418+32C>A	ENSP00000491305.1:n.418+32C>A
ENST00000638952.1:n.897C>A
ENST00000640056.1:c.12C>A	ENSP00000492620.1:p.Gly4=
ENST00000640218.2:c.666C>A MANE Select	ENSP00000491215.1:p.Gly222=
ENST00000640306.1:c.634+32C>A	ENSP00000491685.1:n.634+32C>A
ENST00000640440.1:c.334+32C>A	ENSP00000491263.1:n.334+32C>A
ENST00000649899.1:n.858+32C>A
ENST00000283179.13:c.666C>A	ENSP00000283179.9:p.Gly222=
ENST00000444376.6:c.634+32C>A	ENSP00000393151.2:n.634+32C>A
ENST00000476241.1:n.818+32C>A
NM_004501.3:c.634+32C>A	NP_004492.2:n.634+32C>A
NM_031844.2:c.666C>A	NP_114032.2:p.Gly222=
NM_031844.3:c.666C>A MANE Select	NP_114032.2:p.Gly222=