Canonical Allele Identifier: CA2577021289
Gene: VAMP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85581780A>G , CM000664.2:g.85581780A>G GRCh38
NC_000002.11:g.85808903A>G , CM000664.1:g.85808903A>G GRCh37
NC_000002.10:g.85662414A>G NCBI36
NG_022887.1:g.9290A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263864.10:c.*64A>G MANE Select ENSP00000263864.5:n.*64A>G
ENST00000263864.9:c.*64A>G ENSP00000263864.5:n.*64A>G
ENST00000409760.1:c.*200A>G ENSP00000387094.1:n.*200A>G
ENST00000432071.1:c.*64A>G ENSP00000407984.1:n.*64A>G
NM_003761.4:c.*64A>G NP_003752.2:n.*64A>G
XM_017005170.1:c.*200A>G XP_016860659.1:n.*200A>G
NM_003761.5:c.*64A>G MANE Select NP_003752.2:n.*64A>G