Canonical Allele Identifier: CA2396589581
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888316C= , CM000684.2:g.20888316C= GRCh38
NC_000022.10:g.21242604C= , CM000684.1:g.21242604C= GRCh37
NC_000022.9:g.19572604C= NCBI36
NG_012152.1:g.34313C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*480C= MANE Select ENSP00000215730.6:n.*480C=
ENST00000215730.11:c.*480C= ENSP00000215730.6:n.*480C=
NM_004782.3:c.*480C= NP_004773.1:n.*480C=
NM_004782.4:c.*480C= MANE Select NP_004773.1:n.*480C=