Canonical Allele Identifier: CA2816180531
Gene: SNTA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443540_33443541insTTTCCAAGTTATTAG , CM000682.2:g.33443540_33443541insTTTCCAAGTTATTAG GRCh38
NC_000020.10:g.32031346_32031347insTTTCCAAGTTATTAG , CM000682.1:g.32031346_32031347insTTTCCAAGTTATTAG GRCh37
NC_000020.9:g.31495007_31495008insTTTCCAAGTTATTAG NCBI36
NG_011622.1:g.5352_5353insCTAATAACTTGGAAA , LRG_332:g.5352_5353insCTAATAACTTGGAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.80_81insCTAATAACTTGGAAA MANE Select ENSP00000217381.2:p.Arg28Ter
ENST00000217381.2:c.80_81insCTAATAACTTGGAAA ENSP00000217381.2:p.Arg28Ter
NM_003098.2:c.80_81insCTAATAACTTGGAAA , LRG_332t1:c.80_81insCTAATAACTTGGAAA NP_003089.1:p.Arg28Ter
XM_005260517.1:c.80_81insCTAATAACTTGGAAA XP_005260574.1:p.Arg28Ter
XM_011529007.1:c.80_81insCTAATAACTTGGAAA XP_011527309.1:p.Arg28Ter
XM_011529008.1:c.80_81insCTAATAACTTGGAAA XP_011527310.1:p.Arg28Ter
XR_936612.1:n.313_314insCTAATAACTTGGAAA
NM_003098.3:c.80_81insCTAATAACTTGGAAA MANE Select NP_003089.1:p.Arg28Ter