Canonical Allele Identifier: CA2259497531

Gene: RARA

Linked Data

• dbSNP Id: rs2033140392

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40313787_40313788del , CM000679.2:g.40313787_40313788del	GRCh38
NC_000017.10:g.38470039_38470040del , CM000679.1:g.38470039_38470040del	GRCh37
NC_000017.9:g.35723565_35723566del	NCBI36
NG_027701.1:g.9617_9618del

Transcript Alleles

HGVS	Amino-acid change
ENST00000254066.10:c.-363+4501_-363+4502del MANE Select	ENSP00000254066.5:n.-363+4501_-363+4502de...
ENST00000254066.9:c.-363+4501_-363+4502del	ENSP00000254066.5:n.-363+4501_-363+4502de...
ENST00000577646.5:c.-440+4501_-440+4502del	ENSP00000464287.1:n.-440+4501_-440+4502de...
NM_000964.3:c.-363+4501_-363+4502del	NP_000955.1:n.-363+4501_-363+4502del
XM_011525095.1:c.-440+4501_-440+4502del	XP_011523397.1:n.-440+4501_-440+4502del
NM_000964.4:c.-363+4501_-363+4502del MANE Select	NP_000955.1:n.-363+4501_-363+4502del