Canonical Allele Identifier: CA1231007433
Gene: HNRNPU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244863775C= , CM000663.2:g.244863775C= GRCh38
NC_000001.10:g.245027077C= , CM000663.1:g.245027077C= GRCh37
NC_000001.9:g.243093700C= NCBI36
NG_042184.1:g.5751G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704074.1:c.211G=
ENST00000283179.14:c.533G= ENSP00000283179.10:p.Gly178=
ENST00000444376.7:c.533G= ENSP00000393151.2:p.Gly178=
ENST00000476241.2:n.718G=
ENST00000638475.1:c.317G= ENSP00000491305.1:p.Gly106=
ENST00000638952.1:n.764G=
ENST00000640218.2:c.533G= MANE Select ENSP00000491215.1:p.Gly178=
ENST00000640306.1:c.533G= ENSP00000491685.1:p.Gly178=
ENST00000640440.1:c.233G= ENSP00000491263.1:p.Gly78=
ENST00000649899.1:n.757G=
ENST00000283179.13:c.533G= ENSP00000283179.9:p.Gly178=
ENST00000444376.6:c.533G= ENSP00000393151.2:p.Gly178=
ENST00000476241.1:n.717G=
NM_004501.3:c.533G= NP_004492.2:p.Gly178=
NM_031844.2:c.533G= NP_114032.2:p.Gly178=
NM_031844.3:c.533G= MANE Select NP_114032.2:p.Gly178=