Canonical Allele Identifier: CA2652478040
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33438927_33438928insGT , CM000682.2:g.33438927_33438928insGT GRCh38
NC_000020.10:g.32026733_32026734insGT , CM000682.1:g.32026733_32026734insGT GRCh37
NC_000020.9:g.31490394_31490395insGT NCBI36
NG_011622.1:g.9965_9966insAC , LRG_332:g.9965_9966insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.409_410insAC MANE Select ENSP00000217381.2:p.Ser137TyrfsTer3
ENST00000217381.2:c.409_410insAC ENSP00000217381.2:p.Ser137TyrfsTer3
NM_003098.2:c.409_410insAC , LRG_332t1:c.409_410insAC NP_003089.1:p.Ser137TyrfsTer3
XM_005260517.1:c.409_410insAC XP_005260574.1:p.Ser137TyrfsTer3
XM_011529007.1:c.409_410insAC XP_011527309.1:p.Ser137TyrfsTer3
XM_011529008.1:c.409_410insAC XP_011527310.1:p.Ser137TyrfsTer3
XR_936612.1:n.642_643insAC
XM_024451971.1:c.82_83insAC XP_024307739.1:p.Ser28TyrfsTer3
NM_003098.3:c.409_410insAC MANE Select NP_003089.1:p.Ser137TyrfsTer3