Canonical Allele Identifier: CA2396589668
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888421T= , CM000684.2:g.20888421T= GRCh38
NC_000022.10:g.21242709T= , CM000684.1:g.21242709T= GRCh37
NC_000022.9:g.19572709T= NCBI36
NG_012152.1:g.34418T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*585T= MANE Select ENSP00000215730.6:n.*585T=
ENST00000215730.11:c.*585T= ENSP00000215730.6:n.*585T=
NM_004782.3:c.*585T= NP_004773.1:n.*585T=
NM_004782.4:c.*585T= MANE Select NP_004773.1:n.*585T=