Canonical Allele Identifier: CA345497418

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245027305T>C (hg19) ; chr1:g.244864003T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244864003T>C , CM000663.2:g.244864003T>C	GRCh38
NC_000001.10:g.245027305T>C , CM000663.1:g.245027305T>C	GRCh37
NC_000001.9:g.243093928T>C	NCBI36
NG_042184.1:g.5523A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000283179.14:c.305A>G	ENSP00000283179.10:p.Asp102Gly
ENST00000444376.7:c.305A>G	ENSP00000393151.2:p.Asp102Gly
ENST00000476241.2:n.490A>G
ENST00000638475.1:c.89A>G	ENSP00000491305.1:p.Asp30Gly
ENST00000638952.1:n.536A>G
ENST00000640218.2:c.305A>G MANE Select	ENSP00000491215.1:p.Asp102Gly
ENST00000640306.1:c.305A>G	ENSP00000491685.1:p.Asp102Gly
ENST00000640440.1:c.5A>G	ENSP00000491263.1:p.Asp2Gly
ENST00000649899.1:n.529A>G
ENST00000283179.13:c.305A>G	ENSP00000283179.9:p.Asp102Gly
ENST00000444376.6:c.305A>G	ENSP00000393151.2:p.Asp102Gly
ENST00000476241.1:n.489A>G
NM_004501.3:c.305A>G	NP_004492.2:p.Asp102Gly
NM_031844.2:c.305A>G	NP_114032.2:p.Asp102Gly
NM_031844.3:c.305A>G MANE Select	NP_114032.2:p.Asp102Gly