Canonical Allele Identifier: CA2246165032
Gene: VAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8159364_8159368delinsGAAGA , CM000679.2:g.8159364_8159368delinsGAAGA GRCh38
NC_000017.10:g.8062682_8062686delinsGAAGA , CM000679.1:g.8062682_8062686delinsGAAGA GRCh37
NC_000017.9:g.8003407_8003411delinsGAAGA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316509.11:c.*1487_*1491delinsTCTTC MANE Select ENSP00000314214.6:n.*1487_*1491delinsTCTTC
ENST00000316509.10:c.*1487_*1491delinsTCTTC ENSP00000314214.6:n.*1487_*1491delinsTCTTC
ENST00000498285.1:c.334+2105_334+2109delinsTCTTC ENSP00000464383.1:n.334+2105_334+2109delinsTCTTC
NM_014232.2:c.*1487_*1491delinsTCTTC NP_055047.2:n.*1487_*1491delinsTCTTC
XM_005256775.3:c.*1487_*1491delinsTCTTC XP_005256832.1:n.*1487_*1491delinsTCTTC
NM_001330125.1:c.*1487_*1491delinsTCTTC NP_001317054.1:n.*1487_*1491delinsTCTTC
NM_014232.3:c.*1487_*1491delinsTCTTC MANE Select NP_055047.2:n.*1487_*1491delinsTCTTC