Canonical Allele Identifier: CA2319043601

Gene: RAX2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3770668C= , CM000681.2:g.3770668C=	GRCh38
NC_000019.9:g.3770666C= , CM000681.1:g.3770666C=	GRCh37
NC_000019.8:g.3721666C=	NCBI36
NG_011565.1:g.6554G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000555633.3:c.508G= MANE Select	ENSP00000450456.3:p.Ala170=
ENST00000555633.2:c.508G=	ENSP00000450456.2:p.Ala170=
ENST00000555978.5:c.508G=	ENSP00000450687.2:p.Ala170=
NM_032753.3:c.508G=	NP_116142.1:p.Ala170=
XM_005259662.1:c.646G=	XP_005259719.1:p.Ala216=
NM_001319074.1:c.646G=	NP_001306003.1:p.Ala216=
NM_001319074.4:c.508G= MANE Select	NP_001306003.2:p.Ala170=
NM_032753.4:c.508G=	NP_116142.1:p.Ala170=