Canonical Allele Identifier: CA2652478397
Gene: SNTA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.33443527_33443529dup , CM000682.2:g.33443527_33443529dup GRCh38
NC_000020.10:g.32031333_32031335dup , CM000682.1:g.32031333_32031335dup GRCh37
NC_000020.9:g.31494994_31494996dup NCBI36
NG_011622.1:g.5369_5371dup , LRG_332:g.5369_5371dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000217381.3:c.97_99dup MANE Select ENSP00000217381.2:p.Leu33_Ser34insLeu
ENST00000217381.2:c.97_99dup ENSP00000217381.2:p.Leu33_Ser34insLeu
NM_003098.2:c.97_99dup , LRG_332t1:c.97_99dup NP_003089.1:p.Leu33_Ser34insLeu
XM_005260517.1:c.97_99dup XP_005260574.1:p.Leu33_Ser34insLeu
XM_011529007.1:c.97_99dup XP_011527309.1:p.Leu33_Ser34insLeu
XM_011529008.1:c.97_99dup XP_011527310.1:p.Leu33_Ser34insLeu
XR_936612.1:n.330_332dup
NM_003098.3:c.97_99dup MANE Select NP_003089.1:p.Leu33_Ser34insLeu