Canonical Allele Identifier: CA771906256

Gene: RARA

Linked Data

• dbSNP Id: rs1276314114
• MyVariant Identifiers: chr17:g.38469869T>C (hg19) ; chr17:g.40313617T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40313617T>C , CM000679.2:g.40313617T>C	GRCh38
NC_000017.10:g.38469869T>C , CM000679.1:g.38469869T>C	GRCh37
NC_000017.9:g.35723395T>C	NCBI36
NG_027701.1:g.9447T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.-363+4331T>C MANE Select	ENSP00000254066.5:n.-363+4331T>C
ENST00000254066.9:c.-363+4331T>C	ENSP00000254066.5:n.-363+4331T>C
ENST00000577646.5:c.-440+4331T>C	ENSP00000464287.1:n.-440+4331T>C
NM_000964.3:c.-363+4331T>C	NP_000955.1:n.-363+4331T>C
XM_011525095.1:c.-440+4331T>C	XP_011523397.1:n.-440+4331T>C
NM_000964.4:c.-363+4331T>C MANE Select	NP_000955.1:n.-363+4331T>C