Canonical Allele Identifier: CA2259497556

Gene: RARA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40313826_40313827delinsAC , CM000679.2:g.40313826_40313827delinsAC	GRCh38
NC_000017.10:g.38470078_38470079delinsAC , CM000679.1:g.38470078_38470079delinsAC	GRCh37
NC_000017.9:g.35723604_35723605delinsAC	NCBI36
NG_027701.1:g.9656_9657delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.-363+4540_-363+4541delinsAC MANE Select	ENSP00000254066.5:n.-363+4540_-363+4541delinsAC
ENST00000254066.9:c.-363+4540_-363+4541delinsAC	ENSP00000254066.5:n.-363+4540_-363+4541delinsAC
ENST00000577646.5:c.-440+4540_-440+4541delinsAC	ENSP00000464287.1:n.-440+4540_-440+4541delinsAC
NM_000964.3:c.-363+4540_-363+4541delinsAC	NP_000955.1:n.-363+4540_-363+4541delinsAC
XM_011525095.1:c.-440+4540_-440+4541delinsAC	XP_011523397.1:n.-440+4540_-440+4541delinsAC
NM_000964.4:c.-363+4540_-363+4541delinsAC MANE Select	NP_000955.1:n.-363+4540_-363+4541delinsAC