Canonical Allele Identifier: CA40498442

Gene: HNRNPU

Linked Data

• dbSNP Id: rs954006096
• MyVariant Identifiers: chr1:g.245017761T>G (hg19) ; chr1:g.244854459T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244854459T>G , CM000663.2:g.244854459T>G	GRCh38
NC_000001.10:g.245017761T>G , CM000663.1:g.245017761T>G	GRCh37
NC_000001.9:g.243084384T>G	NCBI36
NG_042184.1:g.15067A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000639628.2:c.1641A>C	ENSP00000491340.1:p.Gly547=
ENST00000704074.1:c.1988A>C
ENST00000283179.14:c.2226A>C	ENSP00000283179.10:p.Gly742=
ENST00000366525.8:n.2082A>C
ENST00000366527.4:n.290A>C
ENST00000440865.2:c.1800A>C	ENSP00000410728.2:p.Gly600=
ENST00000444376.7:c.2412A>C	ENSP00000393151.2:p.Gly804=
ENST00000468690.2:n.5004A>C
ENST00000475997.6:c.411+514A>C	ENSP00000482621.2:n.411+514A>C
ENST00000476241.2:n.4583A>C
ENST00000638230.1:c.1534+514A>C
ENST00000638475.1:c.2178A>C	ENSP00000491305.1:p.Gly726=
ENST00000638716.1:c.1635A>C	ENSP00000491601.1:p.Gly545=
ENST00000638952.1:n.4686A>C
ENST00000639064.1:n.2372A>C
ENST00000639628.1:c.1641A>C	ENSP00000491340.1:p.Gly547=
ENST00000639824.1:c.973A>C
ENST00000639880.1:c.*1405A>C	ENSP00000490988.1:n.*1405A>C
ENST00000640001.1:c.*469A>C	ENSP00000491294.1:n.*469A>C
ENST00000640056.1:c.1792A>C	ENSP00000492620.1:n.1792A>C
ENST00000640218.2:c.2469A>C MANE Select	ENSP00000491215.1:p.Gly823=
ENST00000640264.1:n.246+514A>C
ENST00000640306.1:c.2367+514A>C	ENSP00000491685.1:n.2367+514A>C
ENST00000649899.1:n.2636A>C
ENST00000283179.13:c.2469A>C	ENSP00000283179.9:p.Gly823=
ENST00000366525.7:n.2209A>C
ENST00000444376.6:c.2412A>C	ENSP00000393151.2:p.Gly804=
ENST00000475997.5:c.146+514A>C
ENST00000489705.2:c.45A>C
NM_004501.3:c.2412A>C	NP_004492.2:p.Gly804=
NM_031844.2:c.2469A>C	NP_114032.2:p.Gly823=
NM_031844.3:c.2469A>C MANE Select	NP_114032.2:p.Gly823=