Canonical Allele Identifier: CA743730076
Gene: SNTA1 HGNC NCBI

Linked Data

dbSNP Id: rs1348298062
MyVariant Identifiers: chr20:g.32031511_32031546del (hg19) chr20:g.33443705_33443740del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443706_33443741del , CM000682.2:g.33443706_33443741del GRCh38
NC_000020.10:g.32031512_32031547del , CM000682.1:g.32031512_32031547del GRCh37
NC_000020.9:g.31495173_31495208del NCBI36
NG_011622.1:g.5153_5188del , LRG_332:g.5153_5188del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.-120_-85del MANE Select ENSP00000217381.2:n.-120_-85del
ENST00000217381.2:c.-120_-85del ENSP00000217381.2:n.-120_-85del
NM_003098.2:c.-120_-85del , LRG_332t1:c.-120_-85del NP_003089.1:n.-120_-85del
XM_005260517.1:c.-120_-85del XP_005260574.1:n.-120_-85del
XM_011529007.1:c.-120_-85del XP_011527309.1:n.-120_-85del
XM_011529008.1:c.-120_-85del XP_011527310.1:n.-120_-85del
XR_936612.1:n.114_149del
NM_003098.3:c.-120_-85del MANE Select NP_003089.1:n.-120_-85del
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