Canonical Allele Identifier: CA2259502222

Gene: RARA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40323579C= , CM000679.2:g.40323579C=	GRCh38
NC_000017.10:g.38479831C= , CM000679.1:g.38479831C=	GRCh37
NC_000017.9:g.35733357C=	NCBI36
NG_027701.1:g.19409C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000964.4:c.-362-7278C= MANE Select	NP_000955.1:n.-362-7278C=
ENST00000254066.10:c.-362-7278C= MANE Select	ENSP00000254066.5:n.-362-7278C=
NM_000964.3:c.-362-7278C=	NP_000955.1:n.-362-7278C=
NM_001145301.2:c.-363+5131C=	NP_001138773.1:n.-363+5131C=
NM_001145301.3:c.-363+5131C=	NP_001138773.1:n.-363+5131C=
NM_001145302.2:c.-363+5131C=	NP_001138774.1:n.-363+5131C=
NM_001145302.3:c.-363+5131C=	NP_001138774.1:n.-363+5131C=
ENST00000254066.9:c.-362-7278C=	ENSP00000254066.5:n.-362-7278C=
ENST00000394089.6:c.-363+5131C=	ENSP00000377649.2:n.-363+5131C=
ENST00000425707.7:c.-363+5131C=	ENSP00000389993.3:n.-363+5131C=
ENST00000577646.5:c.-439-2896C=	ENSP00000464287.1:n.-439-2896C=
ENST00000582914.1:n.269+320C=
XM_005257554.1:c.-363+320C=	XP_005257611.1:n.-363+320C=
XM_011525095.1:c.-439-2896C=	XP_011523397.1:n.-439-2896C=
XM_011525591.1:c.25G=	XP_011523893.1:p.Ala9=