Canonical Allele Identifier: CA635293503
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1382795171
gnomAD v2: 20-32026399-TC-T
gnomAD v3: 20-33438593-TC-T
gnomAD v4: 20-33438593-TC-T
MyVariant Identifiers: chr20:g.32026400del (hg19) chr20:g.33438594del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438595del , CM000682.2:g.33438595del GRCh38
NC_000020.10:g.32026401del , CM000682.1:g.32026401del GRCh37
NC_000020.9:g.31490062del NCBI36
NG_011622.1:g.10299del , LRG_332:g.10299del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.496+247del MANE Select ENSP00000217381.2:n.496+247del
ENST00000217381.2:c.496+247del ENSP00000217381.2:n.496+247del
NM_003098.2:c.496+247del , LRG_332t1:c.496+247del NP_003089.1:n.496+247del
XM_005260517.1:c.496+247del XP_005260574.1:n.496+247del
XM_011529007.1:c.496+247del XP_011527309.1:n.496+247del
XM_011529008.1:c.496+247del XP_011527310.1:n.496+247del
XR_936612.1:n.729+247del
XM_024451971.1:c.169+247del XP_024307739.1:n.169+247del
NM_003098.3:c.496+247del MANE Select NP_003089.1:n.496+247del
Search 100 bp 5'
Search 100 bp 3'