Canonical Allele Identifier: CA2396589679
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888444T= , CM000684.2:g.20888444T= GRCh38
NC_000022.10:g.21242732T= , CM000684.1:g.21242732T= GRCh37
NC_000022.9:g.19572732T= NCBI36
NG_012152.1:g.34441T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*608T= MANE Select ENSP00000215730.6:n.*608T=
ENST00000215730.11:c.*608T= ENSP00000215730.6:n.*608T=
NM_004782.3:c.*608T= NP_004773.1:n.*608T=
NM_004782.4:c.*608T= MANE Select NP_004773.1:n.*608T=