Canonical Allele Identifier: CA168987364

Gene: RARRES2

Linked Data

• dbSNP Id: rs773901244
• gnomAD v3: 7-150339509-CTATT-C
• gnomAD v4: 7-150339509-CTATT-C
• MyVariant Identifiers: chr7:g.150036599_150036602del (hg19) ; chr7:g.150339510_150339513del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.150339515_150339518del , CM000669.2:g.150339515_150339518del	GRCh38
NC_000007.13:g.150036604_150036607del , CM000669.1:g.150036604_150036607del	GRCh37
NC_000007.12:g.149667537_149667540del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000223271.8:c.280-432_280-429del MANE Select	ENSP00000223271.3:n.280-432_280-429del
ENST00000223271.7:c.280-432_280-429del	ENSP00000223271.3:n.280-432_280-429del
ENST00000466675.5:c.280-432_280-429del	ENSP00000418009.1:n.280-432_280-429del
ENST00000467793.5:c.280-432_280-429del	ENSP00000417669.1:n.280-432_280-429del
ENST00000478771.2:n.1562-432_1562-429del
ENST00000482669.1:c.280-432_280-429del	ENSP00000418483.1:n.280-432_280-429del
NM_002889.3:c.280-432_280-429del	NP_002880.1:n.280-432_280-429del
XM_017012491.1:c.280-432_280-429del	XP_016867980.1:n.280-432_280-429del
NM_002889.4:c.280-432_280-429del MANE Select	NP_002880.1:n.280-432_280-429del