Canonical Allele Identifier: CA771915759

Gene: RARA

Linked Data

• dbSNP Id: rs1401622253
• MyVariant Identifiers: chr17:g.38489177del (hg19) ; chr17:g.40332925del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.40332926del , CM000679.2:g.40332926del	GRCh38
NC_000017.10:g.38489178del , CM000679.1:g.38489178del	GRCh37
NC_000017.9:g.35742704del	NCBI36
NG_027701.1:g.28756del

Transcript Alleles

HGVS	Amino-acid change
ENST00000254066.10:c.178+1530del MANE Select	ENSP00000254066.5:n.178+1530del
ENST00000254066.9:c.178+1530del	ENSP00000254066.5:n.178+1530del
ENST00000394089.6:c.178+1530del	ENSP00000377649.2:n.178+1530del
ENST00000425707.7:c.178+1530del	ENSP00000389993.3:n.178+1530del
ENST00000577646.5:c.178+1530del	ENSP00000464287.1:n.178+1530del
NM_000964.3:c.178+1530del	NP_000955.1:n.178+1530del
NM_001145301.2:c.178+1530del	NP_001138773.1:n.178+1530del
NM_001145302.2:c.178+1530del	NP_001138774.1:n.178+1530del
XM_005257553.1:c.178+1530del	XP_005257610.1:n.178+1530del
XM_005257554.1:c.178+1530del	XP_005257611.1:n.178+1530del
XM_011525095.1:c.178+1530del	XP_011523397.1:n.178+1530del
NM_000964.4:c.178+1530del MANE Select	NP_000955.1:n.178+1530del
NM_001145301.3:c.178+1530del	NP_001138773.1:n.178+1530del
NM_001145302.3:c.178+1530del	NP_001138774.1:n.178+1530del