Canonical Allele Identifier: CA2259497589

Gene: RARA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40313911_40313914delinsCCCA , CM000679.2:g.40313911_40313914delinsCCCA	GRCh38
NC_000017.10:g.38470163_38470166delinsCCCA , CM000679.1:g.38470163_38470166delinsCCCA	GRCh37
NC_000017.9:g.35723689_35723692delinsCCCA	NCBI36
NG_027701.1:g.9741_9744delinsCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.-363+4625_-363+4628delinsCCCA MANE Select	ENSP00000254066.5:n.-363+4625_-363+4628delinsCCCA
ENST00000254066.9:c.-363+4625_-363+4628delinsCCCA	ENSP00000254066.5:n.-363+4625_-363+4628delinsCCCA
ENST00000577646.5:c.-440+4625_-440+4628delinsCCCA	ENSP00000464287.1:n.-440+4625_-440+4628delinsCCCA
NM_000964.3:c.-363+4625_-363+4628delinsCCCA	NP_000955.1:n.-363+4625_-363+4628delinsCCCA
XM_011525095.1:c.-440+4625_-440+4628delinsCCCA	XP_011523397.1:n.-440+4625_-440+4628delinsCCCA
NM_000964.4:c.-363+4625_-363+4628delinsCCCA MANE Select	NP_000955.1:n.-363+4625_-363+4628delinsCCCA