Canonical Allele Identifier: CA345486211

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245017763C>G (hg19) ; chr1:g.244854461C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244854461C>G , CM000663.2:g.244854461C>G	GRCh38
NC_000001.10:g.245017763C>G , CM000663.1:g.245017763C>G	GRCh37
NC_000001.9:g.243084386C>G	NCBI36
NG_042184.1:g.15065G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000639628.2:c.1639G>C	ENSP00000491340.1:p.Gly547Arg
ENST00000704074.1:c.1986G>C
ENST00000283179.14:c.2224G>C	ENSP00000283179.10:p.Gly742Arg
ENST00000366525.8:n.2080G>C
ENST00000366527.4:n.288G>C
ENST00000440865.2:c.1798G>C	ENSP00000410728.2:p.Gly600Arg
ENST00000444376.7:c.2410G>C	ENSP00000393151.2:p.Gly804Arg
ENST00000468690.2:n.5002G>C
ENST00000475997.6:c.411+512G>C	ENSP00000482621.2:n.411+512G>C
ENST00000476241.2:n.4581G>C
ENST00000638230.1:c.1534+512G>C
ENST00000638475.1:c.2176G>C	ENSP00000491305.1:p.Gly726Arg
ENST00000638716.1:c.1633G>C	ENSP00000491601.1:p.Gly545Arg
ENST00000638952.1:n.4684G>C
ENST00000639064.1:n.2370G>C
ENST00000639628.1:c.1639G>C	ENSP00000491340.1:p.Gly547Arg
ENST00000639824.1:c.971G>C
ENST00000639880.1:c.*1403G>C	ENSP00000490988.1:n.*1403G>C
ENST00000640001.1:c.*467G>C	ENSP00000491294.1:n.*467G>C
ENST00000640056.1:c.1790G>C	ENSP00000492620.1:n.1790G>C
ENST00000640218.2:c.2467G>C MANE Select	ENSP00000491215.1:p.Gly823Arg
ENST00000640264.1:n.246+512G>C
ENST00000640306.1:c.2367+512G>C	ENSP00000491685.1:n.2367+512G>C
ENST00000649899.1:n.2634G>C
ENST00000283179.13:c.2467G>C	ENSP00000283179.9:p.Gly823Arg
ENST00000366525.7:n.2207G>C
ENST00000444376.6:c.2410G>C	ENSP00000393151.2:p.Gly804Arg
ENST00000475997.5:c.146+512G>C
ENST00000489705.2:c.43G>C
NM_004501.3:c.2410G>C	NP_004492.2:p.Gly804Arg
NM_031844.2:c.2467G>C	NP_114032.2:p.Gly823Arg
NM_031844.3:c.2467G>C MANE Select	NP_114032.2:p.Gly823Arg