Canonical Allele Identifier: CA168987386
Gene: RARRES2 HGNC NCBI

Linked Data

dbSNP Id: rs199934549
MyVariant Identifiers: chr7:g.150036622del (hg19) chr7:g.150339533del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.150339533del , CM000669.2:g.150339533del GRCh38
NC_000007.13:g.150036622del , CM000669.1:g.150036622del GRCh37
NC_000007.12:g.149667555del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000223271.8:c.280-452del MANE Select ENSP00000223271.3:n.280-452del
ENST00000223271.7:c.280-452del ENSP00000223271.3:n.280-452del
ENST00000466675.5:c.280-452del ENSP00000418009.1:n.280-452del
ENST00000467793.5:c.280-452del ENSP00000417669.1:n.280-452del
ENST00000478771.2:n.1562-452del
ENST00000482669.1:c.280-452del ENSP00000418483.1:n.280-452del
NM_002889.3:c.280-452del NP_002880.1:n.280-452del
XM_017012491.1:c.280-452del XP_016867980.1:n.280-452del
NM_002889.4:c.280-452del MANE Select NP_002880.1:n.280-452del
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