Canonical Allele Identifier: CA322277711
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs780186197
MyVariant Identifiers: chr22:g.21242638_21242640del (hg19) chr22:g.20888350_20888352del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888350_20888352del , CM000684.2:g.20888350_20888352del GRCh38
NC_000022.10:g.21242638_21242640del , CM000684.1:g.21242638_21242640del GRCh37
NC_000022.9:g.19572638_19572640del NCBI36
NG_012152.1:g.34347_34349del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*514_*516del MANE Select ENSP00000215730.6:n.*514_*516del
ENST00000215730.11:c.*514_*516del ENSP00000215730.6:n.*514_*516del
NM_004782.3:c.*514_*516del NP_004773.1:n.*514_*516del
NM_004782.4:c.*514_*516del MANE Select NP_004773.1:n.*514_*516del
Search 100 bp 5'
Search 100 bp 3'