Canonical Allele Identifier: CA645532141

Gene: HNRNPU

Linked Data

• COSMIC: COSM4517789 ; COSM4517790

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863886_244863887delinsTT , CM000663.2:g.244863886_244863887delinsTT	GRCh38
NC_000001.10:g.245027188_245027189delinsTT , CM000663.1:g.245027188_245027189delinsTT	GRCh37
NC_000001.9:g.243093811_243093812delinsTT	NCBI36
NG_042184.1:g.5639_5640delinsAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.99_100delinsAA
ENST00000283179.14:c.421_422delinsAA	ENSP00000283179.10:p.Gly141Lys
ENST00000444376.7:c.421_422delinsAA	ENSP00000393151.2:p.Gly141Lys
ENST00000476241.2:n.606_607delinsAA
ENST00000638475.1:c.205_206delinsAA	ENSP00000491305.1:p.Gly69Lys
ENST00000638952.1:n.652_653delinsAA
ENST00000640218.2:c.421_422delinsAA MANE Select	ENSP00000491215.1:p.Gly141Lys
ENST00000640306.1:c.421_422delinsAA	ENSP00000491685.1:p.Gly141Lys
ENST00000640440.1:c.121_122delinsAA	ENSP00000491263.1:p.Gly41Lys
ENST00000649899.1:n.645_646delinsAA
ENST00000283179.13:c.421_422delinsAA	ENSP00000283179.9:p.Gly141Lys
ENST00000444376.6:c.421_422delinsAA	ENSP00000393151.2:p.Gly141Lys
ENST00000476241.1:n.605_606delinsAA
NM_004501.3:c.421_422delinsAA	NP_004492.2:p.Gly141Lys
NM_031844.2:c.421_422delinsAA	NP_114032.2:p.Gly141Lys
NM_031844.3:c.421_422delinsAA MANE Select	NP_114032.2:p.Gly141Lys