Canonical Allele Identifier: CA771906265

Gene: RARA

Linked Data

• dbSNP Id: rs1294262536
• gnomAD v3: 17-40313649-A-G
• gnomAD v4: 17-40313649-A-G
• MyVariant Identifiers: chr17:g.38469901A>G (hg19) ; chr17:g.40313649A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40313649A>G , CM000679.2:g.40313649A>G	GRCh38
NC_000017.10:g.38469901A>G , CM000679.1:g.38469901A>G	GRCh37
NC_000017.9:g.35723427A>G	NCBI36
NG_027701.1:g.9479A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.-363+4363A>G MANE Select	ENSP00000254066.5:n.-363+4363A>G
ENST00000254066.9:c.-363+4363A>G	ENSP00000254066.5:n.-363+4363A>G
ENST00000577646.5:c.-440+4363A>G	ENSP00000464287.1:n.-440+4363A>G
NM_000964.3:c.-363+4363A>G	NP_000955.1:n.-363+4363A>G
XM_011525095.1:c.-440+4363A>G	XP_011523397.1:n.-440+4363A>G
NM_000964.4:c.-363+4363A>G MANE Select	NP_000955.1:n.-363+4363A>G