Canonical Allele Identifier: CA424402471

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245026947G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863645G>C , CM000663.2:g.244863645G>C	GRCh38
NC_000001.10:g.245026947G>C , CM000663.1:g.245026947G>C	GRCh37
NC_000001.9:g.243093570G>C	NCBI36
NG_042184.1:g.5881C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.312+29C>G
ENST00000283179.14:c.634+29C>G	ENSP00000283179.10:n.634+29C>G
ENST00000444376.7:c.634+29C>G	ENSP00000393151.2:n.634+29C>G
ENST00000476241.2:n.819+29C>G
ENST00000638475.1:c.418+29C>G	ENSP00000491305.1:n.418+29C>G
ENST00000638952.1:n.894C>G
ENST00000640056.1:c.9C>G	ENSP00000492620.1:p.Gly3=
ENST00000640218.2:c.663C>G MANE Select	ENSP00000491215.1:p.Gly221=
ENST00000640306.1:c.634+29C>G	ENSP00000491685.1:n.634+29C>G
ENST00000640440.1:c.334+29C>G	ENSP00000491263.1:n.334+29C>G
ENST00000649899.1:n.858+29C>G
ENST00000283179.13:c.663C>G	ENSP00000283179.9:p.Gly221=
ENST00000444376.6:c.634+29C>G	ENSP00000393151.2:n.634+29C>G
ENST00000476241.1:n.818+29C>G
NM_004501.3:c.634+29C>G	NP_004492.2:n.634+29C>G
NM_031844.2:c.663C>G	NP_114032.2:p.Gly221=
NM_031844.3:c.663C>G MANE Select	NP_114032.2:p.Gly221=