Canonical Allele Identifier: CA2809462565

Gene: RARA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40313745_40313746insACA , CM000679.2:g.40313745_40313746insACA	GRCh38
NC_000017.10:g.38469997_38469998insACA , CM000679.1:g.38469997_38469998insACA	GRCh37
NC_000017.9:g.35723523_35723524insACA	NCBI36
NG_027701.1:g.9575_9576insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.-363+4459_-363+4460insACA MANE Select	ENSP00000254066.5:n.-363+4459_-363+4460insACA
ENST00000254066.9:c.-363+4459_-363+4460insACA	ENSP00000254066.5:n.-363+4459_-363+4460insACA
ENST00000577646.5:c.-440+4459_-440+4460insACA	ENSP00000464287.1:n.-440+4459_-440+4460insACA
NM_000964.3:c.-363+4459_-363+4460insACA	NP_000955.1:n.-363+4459_-363+4460insACA
XM_011525095.1:c.-440+4459_-440+4460insACA	XP_011523397.1:n.-440+4459_-440+4460insACA
NM_000964.4:c.-363+4459_-363+4460insACA MANE Select	NP_000955.1:n.-363+4459_-363+4460insACA