Canonical Allele Identifier: CA2655449191
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888027del , CM000684.2:g.20888027del GRCh38
NC_000022.10:g.21242315del , CM000684.1:g.21242315del GRCh37
NC_000022.9:g.19572315del NCBI36
NG_012152.1:g.34024del

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*191del MANE Select ENSP00000215730.6:n.*191del
ENST00000215730.11:c.*191del ENSP00000215730.6:n.*191del
NM_004782.3:c.*191del NP_004773.1:n.*191del
NM_004782.4:c.*191del MANE Select NP_004773.1:n.*191del