Canonical Allele Identifier: CA743726929
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1179272958
MyVariant Identifiers: chr20:g.32026379_32026380insA (hg19) chr20:g.33438573_33438574insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438574dup , CM000682.2:g.33438574dup GRCh38
NC_000020.10:g.32026380dup , CM000682.1:g.32026380dup GRCh37
NC_000020.9:g.31490041dup NCBI36
NG_011622.1:g.10319dup , LRG_332:g.10319dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.496+267dup MANE Select ENSP00000217381.2:n.496+267dup
ENST00000217381.2:c.496+267dup ENSP00000217381.2:n.496+267dup
NM_003098.2:c.496+267dup , LRG_332t1:c.496+267dup NP_003089.1:n.496+267dup
XM_005260517.1:c.496+267dup XP_005260574.1:n.496+267dup
XM_011529007.1:c.496+267dup XP_011527309.1:n.496+267dup
XM_011529008.1:c.496+267dup XP_011527310.1:n.496+267dup
XR_936612.1:n.729+267dup
XM_024451971.1:c.169+267dup XP_024307739.1:n.169+267dup
NM_003098.3:c.496+267dup MANE Select NP_003089.1:n.496+267dup
Search 100 bp 5'
Search 100 bp 3'