Canonical Allele Identifier: CA322277413
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs761553472
gnomAD v2: 22-21242222-ATG-A
gnomAD v3: 22-20887934-ATG-A
gnomAD v4: 22-20887934-ATG-A
MyVariant Identifiers: chr22:g.21242223_21242224del (hg19) chr22:g.20887935_20887936del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20887940_20887941del , CM000684.2:g.20887940_20887941del GRCh38
NC_000022.10:g.21242228_21242229del , CM000684.1:g.21242228_21242229del GRCh37
NC_000022.9:g.19572228_19572229del NCBI36
NG_012152.1:g.33937_33938del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*104_*105del MANE Select ENSP00000215730.6:n.*104_*105del
ENST00000215730.11:c.*104_*105del ENSP00000215730.6:n.*104_*105del
NM_004782.3:c.*104_*105del NP_004773.1:n.*104_*105del
NM_004782.4:c.*104_*105del MANE Select NP_004773.1:n.*104_*105del
Search 100 bp 5'
Search 100 bp 3'