Canonical Allele Identifier: CA893994431
Gene: VAMP5 HGNC NCBI

Linked Data

dbSNP Id: rs1329740309
MyVariant Identifiers: chr2:g.85816259_85816273del (hg19) chr2:g.85589136_85589150del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85589141_85589155del , CM000664.2:g.85589141_85589155del GRCh38
NC_000002.11:g.85816264_85816278del , CM000664.1:g.85816264_85816278del GRCh37
NC_000002.10:g.85669775_85669789del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000306384.5:c.4-2584_4-2570del MANE Select ENSP00000305647.4:n.4-2584_4-2570del
ENST00000306384.4:c.4-2584_4-2570del ENSP00000305647.4:n.4-2584_4-2570del
NM_006634.2:c.4-2584_4-2570del NP_006625.1:n.4-2584_4-2570del
NM_006634.3:c.4-2584_4-2570del MANE Select NP_006625.1:n.4-2584_4-2570del
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