Canonical Allele Identifier: CA2655449173
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888000del , CM000684.2:g.20888000del GRCh38
NC_000022.10:g.21242288del , CM000684.1:g.21242288del GRCh37
NC_000022.9:g.19572288del NCBI36
NG_012152.1:g.33997del

Transcript Alleles

HGVS Amino-acid change
ENST00000215730.12:c.*164del MANE Select ENSP00000215730.6:n.*164del
ENST00000215730.11:c.*164del ENSP00000215730.6:n.*164del
NM_004782.3:c.*164del NP_004773.1:n.*164del
NM_004782.4:c.*164del MANE Select NP_004773.1:n.*164del