Canonical Allele Identifier: CA2259502223

Gene: RARA

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.-362-7278C>G MANE Select	ENSP00000254066.5:n.-362-7278C>G
ENST00000254066.9:c.-362-7278C>G	ENSP00000254066.5:n.-362-7278C>G
ENST00000394089.6:c.-363+5131C>G	ENSP00000377649.2:n.-363+5131C>G
ENST00000425707.7:c.-363+5131C>G	ENSP00000389993.3:n.-363+5131C>G
ENST00000577646.5:c.-439-2896C>G	ENSP00000464287.1:n.-439-2896C>G
ENST00000582914.1:n.269+320C>G
NM_000964.3:c.-362-7278C>G	NP_000955.1:n.-362-7278C>G
NM_001145301.2:c.-363+5131C>G	NP_001138773.1:n.-363+5131C>G
NM_001145302.2:c.-363+5131C>G	NP_001138774.1:n.-363+5131C>G
XM_005257554.1:c.-363+320C>G	XP_005257611.1:n.-363+320C>G
XM_011525095.1:c.-439-2896C>G	XP_011523397.1:n.-439-2896C>G
XM_011525591.1:c.25G>C	XP_011523893.1:p.Ala9Pro
NM_000964.4:c.-362-7278C>G MANE Select	NP_000955.1:n.-362-7278C>G
NM_001145301.3:c.-363+5131C>G	NP_001138773.1:n.-363+5131C>G
NM_001145302.3:c.-363+5131C>G	NP_001138774.1:n.-363+5131C>G