Canonical Allele Identifier: CA1266838071
Gene: VAMP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85581763T= , CM000664.2:g.85581763T= GRCh38
NC_000002.11:g.85808886T= , CM000664.1:g.85808886T= GRCh37
NC_000002.10:g.85662397T= NCBI36
NG_022887.1:g.9273T=

Transcript Alleles

HGVS Amino-acid change
ENST00000263864.10:c.*47T= MANE Select ENSP00000263864.5:n.*47T=
ENST00000263864.9:c.*47T= ENSP00000263864.5:n.*47T=
ENST00000409760.1:c.*183T= ENSP00000387094.1:n.*183T=
ENST00000432071.1:c.*47T= ENSP00000407984.1:n.*47T=
NM_003761.4:c.*47T= NP_003752.2:n.*47T=
XM_017005170.1:c.*183T= XP_016860659.1:n.*183T=
NM_003761.5:c.*47T= MANE Select NP_003752.2:n.*47T=