Canonical Allele Identifier: CA345486225

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245017769G>C (hg19) ; chr1:g.244854467G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244854467G>C , CM000663.2:g.244854467G>C	GRCh38
NC_000001.10:g.245017769G>C , CM000663.1:g.245017769G>C	GRCh37
NC_000001.9:g.243084392G>C	NCBI36
NG_042184.1:g.15059C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000639628.2:c.1633C>G	ENSP00000491340.1:p.His545Asp
ENST00000704074.1:c.1980C>G
ENST00000283179.14:c.2218C>G	ENSP00000283179.10:p.His740Asp
ENST00000366525.8:n.2074C>G
ENST00000366527.4:n.282C>G
ENST00000440865.2:c.1792C>G	ENSP00000410728.2:p.His598Asp
ENST00000444376.7:c.2404C>G	ENSP00000393151.2:p.His802Asp
ENST00000468690.2:n.4996C>G
ENST00000475997.6:c.411+506C>G	ENSP00000482621.2:n.411+506C>G
ENST00000476241.2:n.4575C>G
ENST00000638230.1:c.1534+506C>G
ENST00000638475.1:c.2170C>G	ENSP00000491305.1:p.His724Asp
ENST00000638716.1:c.1627C>G	ENSP00000491601.1:p.His543Asp
ENST00000638952.1:n.4678C>G
ENST00000639064.1:n.2364C>G
ENST00000639628.1:c.1633C>G	ENSP00000491340.1:p.His545Asp
ENST00000639824.1:c.965C>G
ENST00000639880.1:c.*1397C>G	ENSP00000490988.1:n.*1397C>G
ENST00000640001.1:c.*461C>G	ENSP00000491294.1:n.*461C>G
ENST00000640056.1:c.1784C>G	ENSP00000492620.1:n.1784C>G
ENST00000640218.2:c.2461C>G MANE Select	ENSP00000491215.1:p.His821Asp
ENST00000640264.1:n.246+506C>G
ENST00000640306.1:c.2367+506C>G	ENSP00000491685.1:n.2367+506C>G
ENST00000649899.1:n.2628C>G
ENST00000283179.13:c.2461C>G	ENSP00000283179.9:p.His821Asp
ENST00000366525.7:n.2201C>G
ENST00000444376.6:c.2404C>G	ENSP00000393151.2:p.His802Asp
ENST00000475997.5:c.146+506C>G
ENST00000489705.2:c.37C>G
NM_004501.3:c.2404C>G	NP_004492.2:p.His802Asp
NM_031844.2:c.2461C>G	NP_114032.2:p.His821Asp
NM_031844.3:c.2461C>G MANE Select	NP_114032.2:p.His821Asp