Canonical Allele Identifier: CA1231007432

Gene: HNRNPU

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.244863771G= , CM000663.2:g.244863771G=	GRCh38
NC_000001.10:g.245027073G= , CM000663.1:g.245027073G=	GRCh37
NC_000001.9:g.243093696G=	NCBI36
NG_042184.1:g.5755C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000704074.1:c.215C=
ENST00000283179.14:c.537C=	ENSP00000283179.10:p.Ala179=
ENST00000444376.7:c.537C=	ENSP00000393151.2:p.Ala179=
ENST00000476241.2:n.722C=
ENST00000638475.1:c.321C=	ENSP00000491305.1:p.Ala107=
ENST00000638952.1:n.768C=
ENST00000640218.2:c.537C= MANE Select	ENSP00000491215.1:p.Ala179=
ENST00000640306.1:c.537C=	ENSP00000491685.1:p.Ala179=
ENST00000640440.1:c.237C=	ENSP00000491263.1:p.Ala79=
ENST00000649899.1:n.761C=
ENST00000283179.13:c.537C=	ENSP00000283179.9:p.Ala179=
ENST00000444376.6:c.537C=	ENSP00000393151.2:p.Ala179=
ENST00000476241.1:n.721C=
NM_004501.3:c.537C=	NP_004492.2:p.Ala179=
NM_031844.2:c.537C=	NP_114032.2:p.Ala179=
NM_031844.3:c.537C= MANE Select	NP_114032.2:p.Ala179=