Canonical Allele Identifier: CA835178394

Gene: RARRES2

Linked Data

• dbSNP Id: rs1390138810
• MyVariant Identifiers: chr7:g.150036593_150036597del (hg19) ; chr7:g.150339504_150339508del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150339509_150339513del , CM000669.2:g.150339509_150339513del	GRCh38
NC_000007.13:g.150036598_150036602del , CM000669.1:g.150036598_150036602del	GRCh37
NC_000007.12:g.149667531_149667535del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223271.8:c.280-427_280-423del MANE Select	ENSP00000223271.3:n.280-427_280-423del
ENST00000223271.7:c.280-427_280-423del	ENSP00000223271.3:n.280-427_280-423del
ENST00000466675.5:c.280-427_280-423del	ENSP00000418009.1:n.280-427_280-423del
ENST00000467793.5:c.280-427_280-423del	ENSP00000417669.1:n.280-427_280-423del
ENST00000478771.2:n.1562-427_1562-423del
ENST00000482669.1:c.280-427_280-423del	ENSP00000418483.1:n.280-427_280-423del
NM_002889.3:c.280-427_280-423del	NP_002880.1:n.280-427_280-423del
XM_017012491.1:c.280-427_280-423del	XP_016867980.1:n.280-427_280-423del
NM_002889.4:c.280-427_280-423del MANE Select	NP_002880.1:n.280-427_280-423del