Canonical Allele Identifier: CA2360743990

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33417813_33417814delinsCA , CM000682.2:g.33417813_33417814delinsCA	GRCh38
NC_000020.10:g.32005619_32005620delinsCA , CM000682.1:g.32005619_32005620delinsCA	GRCh37
NC_000020.9:g.31469280_31469281delinsCA	NCBI36
NG_011622.1:g.31079_31080delinsTG , LRG_332:g.31079_31080delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.606_607delinsTG MANE Select	ENSP00000217381.2:p.Pro202=
ENST00000217381.2:c.606_607delinsTG	ENSP00000217381.2:p.Pro202=
NM_003098.2:c.606_607delinsTG , LRG_332t1:c.606_607delinsTG	NP_003089.1:p.Pro202=
XM_005260517.1:c.606_607delinsTG	XP_005260574.1:p.Pro202=
XM_011529007.1:c.606_607delinsTG	XP_011527309.1:p.Pro202=
XM_011529008.1:c.606_607delinsTG	XP_011527310.1:p.Pro202=
XR_936612.1:n.839_840delinsTG
XM_024451971.1:c.279_280delinsTG	XP_024307739.1:p.Pro93=
NM_003098.3:c.606_607delinsTG MANE Select	NP_003089.1:p.Pro202=