Canonical Allele Identifier: CA1266838121
Gene: VAMP8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85581868C= , CM000664.2:g.85581868C= GRCh38
NC_000002.11:g.85808991C= , CM000664.1:g.85808991C= GRCh37
NC_000002.10:g.85662502C= NCBI36
NG_022887.1:g.9378C=

Transcript Alleles

HGVS Amino-acid change
ENST00000263864.10:c.*152C= MANE Select ENSP00000263864.5:n.*152C=
ENST00000263864.9:c.*152C= ENSP00000263864.5:n.*152C=
ENST00000409760.1:c.*288C= ENSP00000387094.1:n.*288C=
ENST00000432071.1:c.*152C= ENSP00000407984.1:n.*152C=
NM_003761.4:c.*152C= NP_003752.2:n.*152C=
XM_017005170.1:c.*288C= XP_016860659.1:n.*288C=
NM_003761.5:c.*152C= MANE Select NP_003752.2:n.*152C=