Canonical Allele Identifier: CA345497429

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027310G>C (hg19) ; chr1:g.244864008G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864008G>C , CM000663.2:g.244864008G>C	GRCh38
NC_000001.10:g.245027310G>C , CM000663.1:g.245027310G>C	GRCh37
NC_000001.9:g.243093933G>C	NCBI36
NG_042184.1:g.5518C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.300C>G	ENSP00000283179.10:p.Asp100Glu
ENST00000444376.7:c.300C>G	ENSP00000393151.2:p.Asp100Glu
ENST00000476241.2:n.485C>G
ENST00000638475.1:c.84C>G	ENSP00000491305.1:p.Asp28Glu
ENST00000638952.1:n.531C>G
ENST00000640218.2:c.300C>G MANE Select	ENSP00000491215.1:p.Asp100Glu
ENST00000640306.1:c.300C>G	ENSP00000491685.1:p.Asp100Glu
ENST00000649899.1:n.524C>G
ENST00000283179.13:c.300C>G	ENSP00000283179.9:p.Asp100Glu
ENST00000444376.6:c.300C>G	ENSP00000393151.2:p.Asp100Glu
ENST00000476241.1:n.484C>G
NM_004501.3:c.300C>G	NP_004492.2:p.Asp100Glu
NM_031844.2:c.300C>G	NP_114032.2:p.Asp100Glu
NM_031844.3:c.300C>G MANE Select	NP_114032.2:p.Asp100Glu