Canonical Allele Identifier: CA1231007397
Gene: HNRNPU HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244863705G= , CM000663.2:g.244863705G= GRCh38
NC_000001.10:g.245027007G= , CM000663.1:g.245027007G= GRCh37
NC_000001.9:g.243093630G= NCBI36
NG_042184.1:g.5821C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000704074.1:c.281C=
ENST00000283179.14:c.603C= ENSP00000283179.10:p.Pro201=
ENST00000444376.7:c.603C= ENSP00000393151.2:p.Pro201=
ENST00000476241.2:n.788C=
ENST00000638475.1:c.387C= ENSP00000491305.1:p.Pro129=
ENST00000638952.1:n.834C=
ENST00000640218.2:c.603C= MANE Select ENSP00000491215.1:p.Pro201=
ENST00000640306.1:c.603C= ENSP00000491685.1:p.Pro201=
ENST00000640440.1:c.303C= ENSP00000491263.1:p.Pro101=
ENST00000649899.1:n.827C=
ENST00000283179.13:c.603C= ENSP00000283179.9:p.Pro201=
ENST00000444376.6:c.603C= ENSP00000393151.2:p.Pro201=
ENST00000476241.1:n.787C=
NM_004501.3:c.603C= NP_004492.2:p.Pro201=
NM_031844.2:c.603C= NP_114032.2:p.Pro201=
NM_031844.3:c.603C= MANE Select NP_114032.2:p.Pro201=