Canonical Allele Identifier: CA2655449483
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888459_20888460del , CM000684.2:g.20888459_20888460del GRCh38
NC_000022.10:g.21242747_21242748del , CM000684.1:g.21242747_21242748del GRCh37
NC_000022.9:g.19572747_19572748del NCBI36
NG_012152.1:g.34456_34457del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*623_*624del MANE Select ENSP00000215730.6:n.*623_*624del
ENST00000215730.11:c.*623_*624del ENSP00000215730.6:n.*623_*624del
NM_004782.3:c.*623_*624del NP_004773.1:n.*623_*624del
NM_004782.4:c.*623_*624del MANE Select NP_004773.1:n.*623_*624del