Canonical Allele Identifier: CA2652478401
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443535_33443547del , CM000682.2:g.33443535_33443547del GRCh38
NC_000020.10:g.32031341_32031353del , CM000682.1:g.32031341_32031353del GRCh37
NC_000020.9:g.31495002_31495014del NCBI36
NG_011622.1:g.5349_5361del , LRG_332:g.5349_5361del

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.77_89del MANE Select ENSP00000217381.2:p.Glu26GlyfsTer4
ENST00000217381.2:c.77_89del ENSP00000217381.2:p.Glu26GlyfsTer4
NM_003098.2:c.77_89del , LRG_332t1:c.77_89del NP_003089.1:p.Glu26GlyfsTer4
XM_005260517.1:c.77_89del XP_005260574.1:p.Glu26GlyfsTer4
XM_011529007.1:c.77_89del XP_011527309.1:p.Glu26GlyfsTer4
XM_011529008.1:c.77_89del XP_011527310.1:p.Glu26GlyfsTer4
XR_936612.1:n.310_322del
NM_003098.3:c.77_89del MANE Select NP_003089.1:p.Glu26GlyfsTer4