Canonical Allele Identifier: CA2635972745
Gene: VAMP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8159152_8159171del , CM000679.2:g.8159152_8159171del GRCh38
NC_000017.10:g.8062470_8062489del , CM000679.1:g.8062470_8062489del GRCh37
NC_000017.9:g.8003195_8003214del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316509.11:c.*1684_*1703del MANE Select ENSP00000314214.6:n.*1684_*1703del
ENST00000316509.10:c.*1684_*1703del ENSP00000314214.6:n.*1684_*1703del
ENST00000498285.1:c.334+2302_334+2321del ENSP00000464383.1:n.334+2302_334+2321del
NM_014232.2:c.*1684_*1703del NP_055047.2:n.*1684_*1703del
NM_001330125.1:c.*1684_*1703del NP_001317054.1:n.*1684_*1703del
NM_014232.3:c.*1684_*1703del MANE Select NP_055047.2:n.*1684_*1703del