Canonical Allele Identifier: CA2818431154
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888172A>T , CM000684.2:g.20888172A>T GRCh38
NC_000022.10:g.21242460A>T , CM000684.1:g.21242460A>T GRCh37
NC_000022.9:g.19572460A>T NCBI36
NG_012152.1:g.34169A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*336A>T MANE Select ENSP00000215730.6:n.*336A>T
ENST00000215730.11:c.*336A>T ENSP00000215730.6:n.*336A>T
NM_004782.3:c.*336A>T NP_004773.1:n.*336A>T
NM_004782.4:c.*336A>T MANE Select NP_004773.1:n.*336A>T