Canonical Allele Identifier: CA424402548

Gene: HNRNPU

Linked Data

• dbSNP Id: rs1553283828
• MyVariant Identifiers: chr1:g.245027005_245027007del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863703_244863705del , CM000663.2:g.244863703_244863705del	GRCh38
NC_000001.10:g.245027005_245027007del , CM000663.1:g.245027005_245027007del	GRCh37
NC_000001.9:g.243093628_243093630del	NCBI36
NG_042184.1:g.5821_5823del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.281_283del
ENST00000283179.14:c.603_605del	ENSP00000283179.10:p.Gly202del
ENST00000444376.7:c.603_605del	ENSP00000393151.2:p.Gly202del
ENST00000476241.2:n.788_790del
ENST00000638475.1:c.387_389del	ENSP00000491305.1:p.Gly130del
ENST00000638952.1:n.834_836del
ENST00000640218.2:c.603_605del MANE Select	ENSP00000491215.1:p.Gly202del
ENST00000640306.1:c.603_605del	ENSP00000491685.1:p.Gly202del
ENST00000640440.1:c.303_305del	ENSP00000491263.1:p.Gly102del
ENST00000649899.1:n.827_829del
ENST00000283179.13:c.603_605del	ENSP00000283179.9:p.Gly202del
ENST00000444376.6:c.603_605del	ENSP00000393151.2:p.Gly202del
ENST00000476241.1:n.787_789del
NM_004501.3:c.603_605del	NP_004492.2:p.Gly202del
NM_031844.2:c.603_605del	NP_114032.2:p.Gly202del
NM_031844.3:c.603_605del MANE Select	NP_114032.2:p.Gly202del