Canonical Allele Identifier: CA2396589382
Gene: SNAP29 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20887905T= , CM000684.2:g.20887905T= GRCh38
NC_000022.10:g.21242193T= , CM000684.1:g.21242193T= GRCh37
NC_000022.9:g.19572193T= NCBI36
NG_012152.1:g.33902T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*69T= MANE Select ENSP00000215730.6:n.*69T=
ENST00000215730.11:c.*69T= ENSP00000215730.6:n.*69T=
NM_004782.3:c.*69T= NP_004773.1:n.*69T=
NM_004782.4:c.*69T= MANE Select NP_004773.1:n.*69T=
Search 100 bp 5'
Search 100 bp 3'