Canonical Allele Identifier: CA345496713
Gene: HNRNPU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244863785G>A , CM000663.2:g.244863785G>A GRCh38
NC_000001.10:g.245027087G>A , CM000663.1:g.245027087G>A GRCh37
NC_000001.9:g.243093710G>A NCBI36
NG_042184.1:g.5741C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000704074.1:c.201C>T
ENST00000283179.14:c.523C>T ENSP00000283179.10:p.Gln175Ter
ENST00000444376.7:c.523C>T ENSP00000393151.2:p.Gln175Ter
ENST00000476241.2:n.708C>T
ENST00000638475.1:c.307C>T ENSP00000491305.1:p.Gln103Ter
ENST00000638952.1:n.754C>T
ENST00000640218.2:c.523C>T MANE Select ENSP00000491215.1:p.Gln175Ter
ENST00000640306.1:c.523C>T ENSP00000491685.1:p.Gln175Ter
ENST00000640440.1:c.223C>T ENSP00000491263.1:p.Gln75Ter
ENST00000649899.1:n.747C>T
ENST00000283179.13:c.523C>T ENSP00000283179.9:p.Gln175Ter
ENST00000444376.6:c.523C>T ENSP00000393151.2:p.Gln175Ter
ENST00000476241.1:n.707C>T
NM_004501.3:c.523C>T NP_004492.2:p.Gln175Ter
NM_031844.2:c.523C>T NP_114032.2:p.Gln175Ter
NM_031844.3:c.523C>T MANE Select NP_114032.2:p.Gln175Ter