Canonical Allele Identifier: CA1231007484

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863870C= , CM000663.2:g.244863870C=	GRCh38
NC_000001.10:g.245027172C= , CM000663.1:g.245027172C=	GRCh37
NC_000001.9:g.243093795C=	NCBI36
NG_042184.1:g.5656G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.116G=
ENST00000283179.14:c.438G=	ENSP00000283179.10:p.Gly146=
ENST00000444376.7:c.438G=	ENSP00000393151.2:p.Gly146=
ENST00000476241.2:n.623G=
ENST00000638475.1:c.222G=	ENSP00000491305.1:p.Gly74=
ENST00000638952.1:n.669G=
ENST00000640218.2:c.438G= MANE Select	ENSP00000491215.1:p.Gly146=
ENST00000640306.1:c.438G=	ENSP00000491685.1:p.Gly146=
ENST00000640440.1:c.138G=	ENSP00000491263.1:p.Gly46=
ENST00000649899.1:n.662G=
ENST00000283179.13:c.438G=	ENSP00000283179.9:p.Gly146=
ENST00000444376.6:c.438G=	ENSP00000393151.2:p.Gly146=
ENST00000476241.1:n.622G=
NM_004501.3:c.438G=	NP_004492.2:p.Gly146=
NM_031844.2:c.438G=	NP_114032.2:p.Gly146=
NM_031844.3:c.438G= MANE Select	NP_114032.2:p.Gly146=