Canonical Allele Identifier: CA345497441
Gene: HNRNPU HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244864013G>T , CM000663.2:g.244864013G>T GRCh38
NC_000001.10:g.245027315G>T , CM000663.1:g.245027315G>T GRCh37
NC_000001.9:g.243093938G>T NCBI36
NG_042184.1:g.5513C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000283179.14:c.295C>A ENSP00000283179.10:p.Leu99Met
ENST00000444376.7:c.295C>A ENSP00000393151.2:p.Leu99Met
ENST00000476241.2:n.480C>A
ENST00000638475.1:c.79C>A ENSP00000491305.1:p.Leu27Met
ENST00000638952.1:n.526C>A
ENST00000640218.2:c.295C>A MANE Select ENSP00000491215.1:p.Leu99Met
ENST00000640306.1:c.295C>A ENSP00000491685.1:p.Leu99Met
ENST00000649899.1:n.519C>A
ENST00000283179.13:c.295C>A ENSP00000283179.9:p.Leu99Met
ENST00000444376.6:c.295C>A ENSP00000393151.2:p.Leu99Met
ENST00000476241.1:n.479C>A
NM_004501.3:c.295C>A NP_004492.2:p.Leu99Met
NM_031844.2:c.295C>A NP_114032.2:p.Leu99Met
NM_031844.3:c.295C>A MANE Select NP_114032.2:p.Leu99Met