Canonical Allele Identifier: CA2246164911
Gene: VAMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.8159218_8159222delinsTGGGG , CM000679.2:g.8159218_8159222delinsTGGGG GRCh38
NC_000017.10:g.8062536_8062540delinsTGGGG , CM000679.1:g.8062536_8062540delinsTGGGG GRCh37
NC_000017.9:g.8003261_8003265delinsTGGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000316509.11:c.*1633_*1637delinsCCCCA MANE Select ENSP00000314214.6:n.*1633_*1637delinsCCCCA
ENST00000316509.10:c.*1633_*1637delinsCCCCA ENSP00000314214.6:n.*1633_*1637delinsCCCCA
ENST00000498285.1:c.334+2251_334+2255delinsCCCCA ENSP00000464383.1:n.334+2251_334+2255delinsCCCCA
NM_014232.2:c.*1633_*1637delinsCCCCA NP_055047.2:n.*1633_*1637delinsCCCCA
NM_001330125.1:c.*1633_*1637delinsCCCCA NP_001317054.1:n.*1633_*1637delinsCCCCA
NM_014232.3:c.*1633_*1637delinsCCCCA MANE Select NP_055047.2:n.*1633_*1637delinsCCCCA