Canonical Allele Identifier: CA2651343113

Gene: HNRNPU

Linked Data

• gnomAD v4: 1-244863610-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863610C>A , CM000663.2:g.244863610C>A	GRCh38
NC_000001.10:g.245026912C>A , CM000663.1:g.245026912C>A	GRCh37
NC_000001.9:g.243093535C>A	NCBI36
NG_042184.1:g.5916G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.312+64G>T
ENST00000283179.14:c.634+64G>T	ENSP00000283179.10:n.634+64G>T
ENST00000444376.7:c.634+64G>T	ENSP00000393151.2:n.634+64G>T
ENST00000476241.2:n.819+64G>T
ENST00000638475.1:c.418+64G>T	ENSP00000491305.1:n.418+64G>T
ENST00000638952.1:n.922+7G>T
ENST00000640056.1:c.37+7G>T	ENSP00000492620.1:n.37+7G>T
ENST00000640218.2:c.691+7G>T MANE Select	ENSP00000491215.1:n.691+7G>T
ENST00000640306.1:c.634+64G>T	ENSP00000491685.1:n.634+64G>T
ENST00000640440.1:c.334+64G>T	ENSP00000491263.1:n.334+64G>T
ENST00000649899.1:n.858+64G>T
ENST00000283179.13:c.691+7G>T	ENSP00000283179.9:n.691+7G>T
ENST00000444376.6:c.634+64G>T	ENSP00000393151.2:n.634+64G>T
ENST00000476241.1:n.818+64G>T
NM_004501.3:c.634+64G>T	NP_004492.2:n.634+64G>T
NM_031844.2:c.691+7G>T	NP_114032.2:n.691+7G>T
NM_031844.3:c.691+7G>T MANE Select	NP_114032.2:n.691+7G>T