Canonical Allele Identifier: CA2396590074
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20889402T= , CM000684.2:g.20889402T= GRCh38
NC_000022.10:g.21243690T= , CM000684.1:g.21243690T= GRCh37
NC_000022.9:g.19573690T= NCBI36
NG_012152.1:g.35399T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*1566T= MANE Select ENSP00000215730.6:n.*1566T=
ENST00000215730.11:c.*1566T= ENSP00000215730.6:n.*1566T=
NM_004782.3:c.*1566T= NP_004773.1:n.*1566T=
NM_004782.4:c.*1566T= MANE Select NP_004773.1:n.*1566T=