Canonical Allele Identifier: CA424117662

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245017764T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244854462T>C , CM000663.2:g.244854462T>C	GRCh38
NC_000001.10:g.245017764T>C , CM000663.1:g.245017764T>C	GRCh37
NC_000001.9:g.243084387T>C	NCBI36
NG_042184.1:g.15064A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000639628.2:c.1638A>G	ENSP00000491340.1:p.Gln546=
ENST00000704074.1:c.1985A>G
ENST00000283179.14:c.2223A>G	ENSP00000283179.10:p.Gln741=
ENST00000366525.8:n.2079A>G
ENST00000366527.4:n.287A>G
ENST00000440865.2:c.1797A>G	ENSP00000410728.2:p.Gln599=
ENST00000444376.7:c.2409A>G	ENSP00000393151.2:p.Gln803=
ENST00000468690.2:n.5001A>G
ENST00000475997.6:c.411+511A>G	ENSP00000482621.2:n.411+511A>G
ENST00000476241.2:n.4580A>G
ENST00000638230.1:c.1534+511A>G
ENST00000638475.1:c.2175A>G	ENSP00000491305.1:p.Gln725=
ENST00000638716.1:c.1632A>G	ENSP00000491601.1:p.Gln544=
ENST00000638952.1:n.4683A>G
ENST00000639064.1:n.2369A>G
ENST00000639628.1:c.1638A>G	ENSP00000491340.1:p.Gln546=
ENST00000639824.1:c.970A>G
ENST00000639880.1:c.*1402A>G	ENSP00000490988.1:n.*1402A>G
ENST00000640001.1:c.*466A>G	ENSP00000491294.1:n.*466A>G
ENST00000640056.1:c.1789A>G	ENSP00000492620.1:n.1789A>G
ENST00000640218.2:c.2466A>G MANE Select	ENSP00000491215.1:p.Gln822=
ENST00000640264.1:n.246+511A>G
ENST00000640306.1:c.2367+511A>G	ENSP00000491685.1:n.2367+511A>G
ENST00000649899.1:n.2633A>G
ENST00000283179.13:c.2466A>G	ENSP00000283179.9:p.Gln822=
ENST00000366525.7:n.2206A>G
ENST00000444376.6:c.2409A>G	ENSP00000393151.2:p.Gln803=
ENST00000475997.5:c.146+511A>G
ENST00000489705.2:c.42A>G
NM_004501.3:c.2409A>G	NP_004492.2:p.Gln803=
NM_031844.2:c.2466A>G	NP_114032.2:p.Gln822=
NM_031844.3:c.2466A>G MANE Select	NP_114032.2:p.Gln822=