Canonical Allele Identifier: CA743726946
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1317096810
MyVariant Identifiers: chr20:g.32026430del (hg19) chr20:g.33438624del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438624del , CM000682.2:g.33438624del GRCh38
NC_000020.10:g.32026430del , CM000682.1:g.32026430del GRCh37
NC_000020.9:g.31490091del NCBI36
NG_011622.1:g.10269del , LRG_332:g.10269del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.496+217del MANE Select ENSP00000217381.2:n.496+217del
ENST00000217381.2:c.496+217del ENSP00000217381.2:n.496+217del
NM_003098.2:c.496+217del , LRG_332t1:c.496+217del NP_003089.1:n.496+217del
XM_005260517.1:c.496+217del XP_005260574.1:n.496+217del
XM_011529007.1:c.496+217del XP_011527309.1:n.496+217del
XM_011529008.1:c.496+217del XP_011527310.1:n.496+217del
XR_936612.1:n.729+217del
XM_024451971.1:c.169+217del XP_024307739.1:n.169+217del
NM_003098.3:c.496+217del MANE Select NP_003089.1:n.496+217del
Search 100 bp 5'
Search 100 bp 3'