Canonical Allele Identifier: CA638542812
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs1929068802
gnomAD v2: 22-21242598-T-TACACACACACACACACAC
gnomAD v3: 22-20888310-T-TACACACACACACACACAC
gnomAD v4: 22-20888310-T-TACACACACACACACACAC
MyVariant Identifiers: chr22:g.21242599_21242603delinsACACACACACACACACACTCACA (hg19) chr22:g.20888311_20888315delinsACACACACACACACACACTCACA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888310_20888311insACACACACACACACACAC , CM000684.2:g.20888310_20888311insACACACACACACACACAC GRCh38
NC_000022.10:g.21242598_21242599insACACACACACACACACAC , CM000684.1:g.21242598_21242599insACACACACACACACACAC GRCh37
NC_000022.9:g.19572598_19572599insACACACACACACACACAC NCBI36
NG_012152.1:g.34307_34308insACACACACACACACACAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*474_*475insACACACACACACACACAC MANE Select ENSP00000215730.6:n.*474_*475insACACACACACACACACAC
ENST00000215730.11:c.*474_*475insACACACACACACACACAC ENSP00000215730.6:n.*474_*475insACACACACACACACACAC
NM_004782.3:c.*474_*475insACACACACACACACACAC NP_004773.1:n.*474_*475insACACACACACACACACAC
NM_004782.4:c.*474_*475insACACACACACACACACAC MANE Select NP_004773.1:n.*474_*475insACACACACACACACACAC
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