Canonical Allele Identifier: CA919839694

Gene: RARA

Linked Data

• dbSNP Id: rs1567742252

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40313702_40313704del , CM000679.2:g.40313702_40313704del	GRCh38
NC_000017.10:g.38469954_38469956del , CM000679.1:g.38469954_38469956del	GRCh37
NC_000017.9:g.35723480_35723482del	NCBI36
NG_027701.1:g.9532_9534del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.-363+4416_-363+4418del MANE Select	ENSP00000254066.5:n.-363+4416_-363+4418del
ENST00000254066.9:c.-363+4416_-363+4418del	ENSP00000254066.5:n.-363+4416_-363+4418del
ENST00000577646.5:c.-440+4416_-440+4418del	ENSP00000464287.1:n.-440+4416_-440+4418del
NM_000964.3:c.-363+4416_-363+4418del	NP_000955.1:n.-363+4416_-363+4418del
XM_011525095.1:c.-440+4416_-440+4418del	XP_011523397.1:n.-440+4416_-440+4418del
NM_000964.4:c.-363+4416_-363+4418del MANE Select	NP_000955.1:n.-363+4416_-363+4418del