Canonical Allele Identifier: CA2396589476
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888109A= , CM000684.2:g.20888109A= GRCh38
NC_000022.10:g.21242397A= , CM000684.1:g.21242397A= GRCh37
NC_000022.9:g.19572397A= NCBI36
NG_012152.1:g.34106A=

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*273A= MANE Select ENSP00000215730.6:n.*273A=
ENST00000215730.11:c.*273A= ENSP00000215730.6:n.*273A=
NM_004782.3:c.*273A= NP_004773.1:n.*273A=
NM_004782.4:c.*273A= MANE Select NP_004773.1:n.*273A=