Canonical Allele Identifier: CA2396589594
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888330C= , CM000684.2:g.20888330C= GRCh38
NC_000022.10:g.21242618C= , CM000684.1:g.21242618C= GRCh37
NC_000022.9:g.19572618C= NCBI36
NG_012152.1:g.34327C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*494C= MANE Select ENSP00000215730.6:n.*494C=
ENST00000215730.11:c.*494C= ENSP00000215730.6:n.*494C=
NM_004782.3:c.*494C= NP_004773.1:n.*494C=
NM_004782.4:c.*494C= MANE Select NP_004773.1:n.*494C=