Canonical Allele Identifier: CA771915817

Gene: RARA

Linked Data

• dbSNP Id: rs1479110312
• gnomAD v3: 17-40333072-CAG-C
• gnomAD v4: 17-40333072-CAG-C
• MyVariant Identifiers: chr17:g.38489325_38489326del (hg19) ; chr17:g.40333073_40333074del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40333075_40333076del , CM000679.2:g.40333075_40333076del	GRCh38
NC_000017.10:g.38489327_38489328del , CM000679.1:g.38489327_38489328del	GRCh37
NC_000017.9:g.35742853_35742854del	NCBI36
NG_027701.1:g.28905_28906del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254066.10:c.178+1679_178+1680del MANE Select	ENSP00000254066.5:n.178+1679_178+1680del
ENST00000254066.9:c.178+1679_178+1680del	ENSP00000254066.5:n.178+1679_178+1680del
ENST00000394089.6:c.178+1679_178+1680del	ENSP00000377649.2:n.178+1679_178+1680del
ENST00000425707.7:c.178+1679_178+1680del	ENSP00000389993.3:n.178+1679_178+1680del
ENST00000577646.5:c.178+1679_178+1680del	ENSP00000464287.1:n.178+1679_178+1680del
NM_000964.3:c.178+1679_178+1680del	NP_000955.1:n.178+1679_178+1680del
NM_001145301.2:c.178+1679_178+1680del	NP_001138773.1:n.178+1679_178+1680del
NM_001145302.2:c.178+1679_178+1680del	NP_001138774.1:n.178+1679_178+1680del
XM_005257553.1:c.178+1679_178+1680del	XP_005257610.1:n.178+1679_178+1680del
XM_005257554.1:c.178+1679_178+1680del	XP_005257611.1:n.178+1679_178+1680del
XM_011525095.1:c.178+1679_178+1680del	XP_011523397.1:n.178+1679_178+1680del
NM_000964.4:c.178+1679_178+1680del MANE Select	NP_000955.1:n.178+1679_178+1680del
NM_001145301.3:c.178+1679_178+1680del	NP_001138773.1:n.178+1679_178+1680del
NM_001145302.3:c.178+1679_178+1680del	NP_001138774.1:n.178+1679_178+1680del