Canonical Allele Identifier: CA2259497488

Gene: RARA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40313699_40313702delinsTCTC , CM000679.2:g.40313699_40313702delinsTCTC	GRCh38
NC_000017.10:g.38469951_38469954delinsTCTC , CM000679.1:g.38469951_38469954delinsTCTC	GRCh37
NC_000017.9:g.35723477_35723480delinsTCTC	NCBI36
NG_027701.1:g.9529_9532delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.-363+4413_-363+4416delinsTCTC MANE Select	ENSP00000254066.5:n.-363+4413_-363+4416delinsTCTC
ENST00000254066.9:c.-363+4413_-363+4416delinsTCTC	ENSP00000254066.5:n.-363+4413_-363+4416delinsTCTC
ENST00000577646.5:c.-440+4413_-440+4416delinsTCTC	ENSP00000464287.1:n.-440+4413_-440+4416delinsTCTC
NM_000964.3:c.-363+4413_-363+4416delinsTCTC	NP_000955.1:n.-363+4413_-363+4416delinsTCTC
XM_011525095.1:c.-440+4413_-440+4416delinsTCTC	XP_011523397.1:n.-440+4413_-440+4416delinsTCTC
NM_000964.4:c.-363+4413_-363+4416delinsTCTC MANE Select	NP_000955.1:n.-363+4413_-363+4416delinsTCTC