Canonical Allele Identifier: CA345486200

Gene: HNRNPU

Linked Data

• MyVariant Identifiers: chr1:g.245017758A>C (hg19) ; chr1:g.244854456A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244854456A>C , CM000663.2:g.244854456A>C	GRCh38
NC_000001.10:g.245017758A>C , CM000663.1:g.245017758A>C	GRCh37
NC_000001.9:g.243084381A>C	NCBI36
NG_042184.1:g.15070T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000639628.2:c.1644T>G	ENSP00000491340.1:p.Tyr548Ter
ENST00000704074.1:c.1991T>G
ENST00000283179.14:c.2229T>G	ENSP00000283179.10:p.Tyr743Ter
ENST00000366525.8:n.2085T>G
ENST00000366527.4:n.293T>G
ENST00000440865.2:c.1803T>G	ENSP00000410728.2:p.Tyr601Ter
ENST00000444376.7:c.2415T>G	ENSP00000393151.2:p.Tyr805Ter
ENST00000468690.2:n.5007T>G
ENST00000475997.6:c.411+517T>G	ENSP00000482621.2:n.411+517T>G
ENST00000476241.2:n.4586T>G
ENST00000638230.1:c.1534+517T>G
ENST00000638475.1:c.2181T>G	ENSP00000491305.1:p.Tyr727Ter
ENST00000638716.1:c.1638T>G	ENSP00000491601.1:p.Tyr546Ter
ENST00000638952.1:n.4689T>G
ENST00000639064.1:n.2375T>G
ENST00000639628.1:c.1644T>G	ENSP00000491340.1:p.Tyr548Ter
ENST00000639824.1:c.976T>G
ENST00000639880.1:c.*1408T>G	ENSP00000490988.1:n.*1408T>G
ENST00000640001.1:c.*472T>G	ENSP00000491294.1:n.*472T>G
ENST00000640056.1:c.1795T>G	ENSP00000492620.1:n.1795T>G
ENST00000640218.2:c.2472T>G MANE Select	ENSP00000491215.1:p.Tyr824Ter
ENST00000640264.1:n.246+517T>G
ENST00000640306.1:c.2367+517T>G	ENSP00000491685.1:n.2367+517T>G
ENST00000649899.1:n.2639T>G
ENST00000283179.13:c.2472T>G	ENSP00000283179.9:p.Tyr824Ter
ENST00000366525.7:n.2212T>G
ENST00000444376.6:c.2415T>G	ENSP00000393151.2:p.Tyr805Ter
ENST00000475997.5:c.146+517T>G
ENST00000489705.2:c.48T>G
NM_004501.3:c.2415T>G	NP_004492.2:p.Tyr805Ter
NM_031844.2:c.2472T>G	NP_114032.2:p.Tyr824Ter
NM_031844.3:c.2472T>G MANE Select	NP_114032.2:p.Tyr824Ter