Canonical Allele Identifier: CA2499883981
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888065_20888066del , CM000684.2:g.20888065_20888066del GRCh38
NC_000022.10:g.21242353_21242354del , CM000684.1:g.21242353_21242354del GRCh37
NC_000022.9:g.19572353_19572354del NCBI36
NG_012152.1:g.34062_34063del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*229_*230del MANE Select ENSP00000215730.6:n.*229_*230del
ENST00000215730.11:c.*229_*230del ENSP00000215730.6:n.*229_*230del
NM_004782.3:c.*229_*230del NP_004773.1:n.*229_*230del
NM_004782.4:c.*229_*230del MANE Select NP_004773.1:n.*229_*230del