Canonical Allele Identifier: CA2396589669
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888422A= , CM000684.2:g.20888422A= GRCh38
NC_000022.10:g.21242710A= , CM000684.1:g.21242710A= GRCh37
NC_000022.9:g.19572710A= NCBI36
NG_012152.1:g.34419A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*586A= MANE Select ENSP00000215730.6:n.*586A=
ENST00000215730.11:c.*586A= ENSP00000215730.6:n.*586A=
NM_004782.3:c.*586A= NP_004773.1:n.*586A=
NM_004782.4:c.*586A= MANE Select NP_004773.1:n.*586A=