Canonical Allele Identifier: CA1231007486

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863872C= , CM000663.2:g.244863872C=	GRCh38
NC_000001.10:g.245027174C= , CM000663.1:g.245027174C=	GRCh37
NC_000001.9:g.243093797C=	NCBI36
NG_042184.1:g.5654G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000704074.1:c.114G=
ENST00000283179.14:c.436G=	ENSP00000283179.10:p.Gly146=
ENST00000444376.7:c.436G=	ENSP00000393151.2:p.Gly146=
ENST00000476241.2:n.621G=
ENST00000638475.1:c.220G=	ENSP00000491305.1:p.Gly74=
ENST00000638952.1:n.667G=
ENST00000640218.2:c.436G= MANE Select	ENSP00000491215.1:p.Gly146=
ENST00000640306.1:c.436G=	ENSP00000491685.1:p.Gly146=
ENST00000640440.1:c.136G=	ENSP00000491263.1:p.Gly46=
ENST00000649899.1:n.660G=
ENST00000283179.13:c.436G=	ENSP00000283179.9:p.Gly146=
ENST00000444376.6:c.436G=	ENSP00000393151.2:p.Gly146=
ENST00000476241.1:n.620G=
NM_004501.3:c.436G=	NP_004492.2:p.Gly146=
NM_031844.2:c.436G=	NP_114032.2:p.Gly146=
NM_031844.3:c.436G= MANE Select	NP_114032.2:p.Gly146=