Canonical Allele Identifier: CA2655449390
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888351_20888360del , CM000684.2:g.20888351_20888360del GRCh38
NC_000022.10:g.21242639_21242648del , CM000684.1:g.21242639_21242648del GRCh37
NC_000022.9:g.19572639_19572648del NCBI36
NG_012152.1:g.34348_34357del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*515_*524del MANE Select ENSP00000215730.6:n.*515_*524del
ENST00000215730.11:c.*515_*524del ENSP00000215730.6:n.*515_*524del
NM_004782.3:c.*515_*524del NP_004773.1:n.*515_*524del
NM_004782.4:c.*515_*524del MANE Select NP_004773.1:n.*515_*524del