Canonical Allele Identifier: CA2360741622

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33412226_33412228delinsCTT , CM000682.2:g.33412226_33412228delinsCTT	GRCh38
NC_000020.10:g.32000032_32000034delinsCTT , CM000682.1:g.32000032_32000034delinsCTT	GRCh37
NC_000020.9:g.31463693_31463695delinsCTT	NCBI36
NG_011622.1:g.36665_36667delinsAAG , LRG_332:g.36665_36667delinsAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.1040+68_1040+70delinsAAG MANE Select	ENSP00000217381.2:n.1040+68_1040+70delinsAAG
ENST00000217381.2:c.1040+68_1040+70delinsAAG	ENSP00000217381.2:n.1040+68_1040+70delinsAAG
NM_003098.2:c.1040+68_1040+70delinsAAG , LRG_332t1:c.1040+68_1040+70delinsAAG	NP_003089.1:n.1040+68_1040+70delinsAAG
XM_005260517.1:c.1040+68_1040+70delinsAAG	XP_005260574.1:n.1040+68_1040+70delinsAAG
XM_011529007.1:c.1040+68_1040+70delinsAAG	XP_011527309.1:n.1040+68_1040+70delinsAAG
XM_011529008.1:c.1040+68_1040+70delinsAAG	XP_011527310.1:n.1040+68_1040+70delinsAAG
XR_936612.1:n.1273+68_1273+70delinsAAG
XM_024451971.1:c.713+68_713+70delinsAAG	XP_024307739.1:n.713+68_713+70delinsAAG
NM_003098.3:c.1040+68_1040+70delinsAAG MANE Select	NP_003089.1:n.1040+68_1040+70delinsAAG