Canonical Allele Identifier: CA2360754995

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33443544_33443546delinsTCG , CM000682.2:g.33443544_33443546delinsTCG	GRCh38
NC_000020.10:g.32031350_32031352delinsTCG , CM000682.1:g.32031350_32031352delinsTCG	GRCh37
NC_000020.9:g.31495011_31495013delinsTCG	NCBI36
NG_011622.1:g.5347_5349delinsCGA , LRG_332:g.5347_5349delinsCGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.75_77delinsCGA MANE Select	ENSP00000217381.2:p.Gly25=
ENST00000217381.2:c.75_77delinsCGA	ENSP00000217381.2:p.Gly25=
NM_003098.2:c.75_77delinsCGA , LRG_332t1:c.75_77delinsCGA	NP_003089.1:p.Gly25=
XM_005260517.1:c.75_77delinsCGA	XP_005260574.1:p.Gly25=
XM_011529007.1:c.75_77delinsCGA	XP_011527309.1:p.Gly25=
XM_011529008.1:c.75_77delinsCGA	XP_011527310.1:p.Gly25=
XR_936612.1:n.308_310delinsCGA
NM_003098.3:c.75_77delinsCGA MANE Select	NP_003089.1:p.Gly25=