Canonical Allele Identifier: CA2396589413
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20887995G= , CM000684.2:g.20887995G= GRCh38
NC_000022.10:g.21242283G= , CM000684.1:g.21242283G= GRCh37
NC_000022.9:g.19572283G= NCBI36
NG_012152.1:g.33992G=

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*159G= MANE Select ENSP00000215730.6:n.*159G=
ENST00000215730.11:c.*159G= ENSP00000215730.6:n.*159G=
NM_004782.3:c.*159G= NP_004773.1:n.*159G=
NM_004782.4:c.*159G= MANE Select NP_004773.1:n.*159G=