Canonical Allele Identifier: CA2360752943

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438544_33438546delinsCCT , CM000682.2:g.33438544_33438546delinsCCT	GRCh38
NC_000020.10:g.32026350_32026352delinsCCT , CM000682.1:g.32026350_32026352delinsCCT	GRCh37
NC_000020.9:g.31490011_31490013delinsCCT	NCBI36
NG_011622.1:g.10347_10349delinsAGG , LRG_332:g.10347_10349delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+295_496+297delinsAGG MANE Select	ENSP00000217381.2:n.496+295_496+297delinsAGG
ENST00000217381.2:c.496+295_496+297delinsAGG	ENSP00000217381.2:n.496+295_496+297delinsAGG
NM_003098.2:c.496+295_496+297delinsAGG , LRG_332t1:c.496+295_496+297delinsAGG	NP_003089.1:n.496+295_496+297delinsAGG
XM_005260517.1:c.496+295_496+297delinsAGG	XP_005260574.1:n.496+295_496+297delinsAGG
XM_011529007.1:c.496+295_496+297delinsAGG	XP_011527309.1:n.496+295_496+297delinsAGG
XM_011529008.1:c.496+295_496+297delinsAGG	XP_011527310.1:n.496+295_496+297delinsAGG
XR_936612.1:n.729+295_729+297delinsAGG
XM_024451971.1:c.169+295_169+297delinsAGG	XP_024307739.1:n.169+295_169+297delinsAGG
NM_003098.3:c.496+295_496+297delinsAGG MANE Select	NP_003089.1:n.496+295_496+297delinsAGG