Canonical Allele Identifier: CA345496796

Gene: HNRNPU

Linked Data

• dbSNP Id: rs1680924291
• MyVariant Identifiers: chr1:g.245027104T>G (hg19) ; chr1:g.244863802T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863802T>G , CM000663.2:g.244863802T>G	GRCh38
NC_000001.10:g.245027104T>G , CM000663.1:g.245027104T>G	GRCh37
NC_000001.9:g.243093727T>G	NCBI36
NG_042184.1:g.5724A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.184A>C
ENST00000283179.14:c.506A>C	ENSP00000283179.10:p.Gln169Pro
ENST00000444376.7:c.506A>C	ENSP00000393151.2:p.Gln169Pro
ENST00000476241.2:n.691A>C
ENST00000638475.1:c.290A>C	ENSP00000491305.1:p.Gln97Pro
ENST00000638952.1:n.737A>C
ENST00000640218.2:c.506A>C MANE Select	ENSP00000491215.1:p.Gln169Pro
ENST00000640306.1:c.506A>C	ENSP00000491685.1:p.Gln169Pro
ENST00000640440.1:c.206A>C	ENSP00000491263.1:p.Gln69Pro
ENST00000649899.1:n.730A>C
ENST00000283179.13:c.506A>C	ENSP00000283179.9:p.Gln169Pro
ENST00000444376.6:c.506A>C	ENSP00000393151.2:p.Gln169Pro
ENST00000476241.1:n.690A>C
NM_004501.3:c.506A>C	NP_004492.2:p.Gln169Pro
NM_031844.2:c.506A>C	NP_114032.2:p.Gln169Pro
NM_031844.3:c.506A>C MANE Select	NP_114032.2:p.Gln169Pro