Canonical Allele Identifier: CA771906340

Gene: RARA

Linked Data

• dbSNP Id: rs1414052375
• MyVariant Identifiers: chr17:g.38470164_38470166del (hg19) ; chr17:g.40313912_40313914del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40313915_40313917del , CM000679.2:g.40313915_40313917del	GRCh38
NC_000017.10:g.38470167_38470169del , CM000679.1:g.38470167_38470169del	GRCh37
NC_000017.9:g.35723693_35723695del	NCBI36
NG_027701.1:g.9745_9747del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.-363+4629_-363+4631del MANE Select	ENSP00000254066.5:n.-363+4629_-363+4631del
ENST00000254066.9:c.-363+4629_-363+4631del	ENSP00000254066.5:n.-363+4629_-363+4631del
ENST00000577646.5:c.-440+4629_-440+4631del	ENSP00000464287.1:n.-440+4629_-440+4631del
NM_000964.3:c.-363+4629_-363+4631del	NP_000955.1:n.-363+4629_-363+4631del
XM_011525095.1:c.-440+4629_-440+4631del	XP_011523397.1:n.-440+4629_-440+4631del
NM_000964.4:c.-363+4629_-363+4631del MANE Select	NP_000955.1:n.-363+4629_-363+4631del