Canonical Allele Identifier: CA2655449537
Gene: SNAP29 HGNC NCBI

Linked Data

gnomAD v4: 22-20888499-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888500del , CM000684.2:g.20888500del GRCh38
NC_000022.10:g.21242788del , CM000684.1:g.21242788del GRCh37
NC_000022.9:g.19572788del NCBI36
NG_012152.1:g.34497del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*664del MANE Select ENSP00000215730.6:n.*664del
ENST00000215730.11:c.*664del ENSP00000215730.6:n.*664del
NM_004782.3:c.*664del NP_004773.1:n.*664del
NM_004782.4:c.*664del MANE Select NP_004773.1:n.*664del
Search 100 bp 5'
Search 100 bp 3'