Canonical Allele Identifier: CA656631104

Gene: RARA

Linked Data

• COSMIC: COSN23988235

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40332975G>A , CM000679.2:g.40332975G>A	GRCh38
NC_000017.10:g.38489227G>A , CM000679.1:g.38489227G>A	GRCh37
NC_000017.9:g.35742753G>A	NCBI36
NG_027701.1:g.28805G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000254066.10:c.178+1579G>A MANE Select	ENSP00000254066.5:n.178+1579G>A
ENST00000254066.9:c.178+1579G>A	ENSP00000254066.5:n.178+1579G>A
ENST00000394089.6:c.178+1579G>A	ENSP00000377649.2:n.178+1579G>A
ENST00000425707.7:c.178+1579G>A	ENSP00000389993.3:n.178+1579G>A
ENST00000577646.5:c.178+1579G>A	ENSP00000464287.1:n.178+1579G>A
NM_000964.3:c.178+1579G>A	NP_000955.1:n.178+1579G>A
NM_001145301.2:c.178+1579G>A	NP_001138773.1:n.178+1579G>A
NM_001145302.2:c.178+1579G>A	NP_001138774.1:n.178+1579G>A
XM_005257553.1:c.178+1579G>A	XP_005257610.1:n.178+1579G>A
XM_005257554.1:c.178+1579G>A	XP_005257611.1:n.178+1579G>A
XM_011525095.1:c.178+1579G>A	XP_011523397.1:n.178+1579G>A
NM_000964.4:c.178+1579G>A MANE Select	NP_000955.1:n.178+1579G>A
NM_001145301.3:c.178+1579G>A	NP_001138773.1:n.178+1579G>A
NM_001145302.3:c.178+1579G>A	NP_001138774.1:n.178+1579G>A