Canonical Allele Identifier: CA2259514933

Gene: RARA

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40351852G>A , CM000679.2:g.40351852G>A	GRCh38
NC_000017.10:g.38508104G>A , CM000679.1:g.38508104G>A	GRCh37
NC_000017.9:g.35761630G>A	NCBI36
NG_027701.1:g.47682G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.470-58G>A MANE Select	ENSP00000254066.5:n.470-58G>A
ENST00000254066.9:c.470-58G>A	ENSP00000254066.5:n.470-58G>A
ENST00000394081.7:c.455-58G>A	ENSP00000377643.3:n.455-58G>A
ENST00000394086.7:c.518-58G>A	ENSP00000377648.3:n.518-58G>A
ENST00000394089.6:c.470-58G>A	ENSP00000377649.2:n.470-58G>A
ENST00000420042.1:n.146-58G>A
ENST00000425707.7:c.179-58G>A	ENSP00000389993.3:n.179-58G>A
ENST00000475125.1:c.113-58G>A	ENSP00000462514.1:n.113-58G>A
NM_000964.3:c.470-58G>A	NP_000955.1:n.470-58G>A
NM_001024809.3:c.455-58G>A	NP_001019980.1:n.455-58G>A
NM_001145301.2:c.470-58G>A	NP_001138773.1:n.470-58G>A
NM_001145302.2:c.179-58G>A	NP_001138774.1:n.179-58G>A
XM_005257552.3:c.518-58G>A	XP_005257609.1:n.518-58G>A
XM_005257553.1:c.470-58G>A	XP_005257610.1:n.470-58G>A
XM_005257554.1:c.470-58G>A	XP_005257611.1:n.470-58G>A
XM_011525095.1:c.470-58G>A	XP_011523397.1:n.470-58G>A
XM_011525096.1:c.296-58G>A	XP_011523398.1:n.296-58G>A
XM_005257552.5:c.518-58G>A	XP_005257609.1:n.518-58G>A
XM_017024920.2:c.113-58G>A	XP_016880409.1:n.113-58G>A
NM_000964.4:c.470-58G>A MANE Select	NP_000955.1:n.470-58G>A
NM_001024809.4:c.455-58G>A	NP_001019980.1:n.455-58G>A
NM_001145301.3:c.470-58G>A	NP_001138773.1:n.470-58G>A
NM_001145302.3:c.179-58G>A	NP_001138774.1:n.179-58G>A