Canonical Allele Identifier: CA2652477931

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33438697-TCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438700_33438701del , CM000682.2:g.33438700_33438701del	GRCh38
NC_000020.10:g.32026506_32026507del , CM000682.1:g.32026506_32026507del	GRCh37
NC_000020.9:g.31490167_31490168del	NCBI36
NG_011622.1:g.10194_10195del , LRG_332:g.10194_10195del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+142_496+143del MANE Select	ENSP00000217381.2:n.496+142_496+143del
ENST00000217381.2:c.496+142_496+143del	ENSP00000217381.2:n.496+142_496+143del
NM_003098.2:c.496+142_496+143del , LRG_332t1:c.496+142_496+143del	NP_003089.1:n.496+142_496+143del
XM_005260517.1:c.496+142_496+143del	XP_005260574.1:n.496+142_496+143del
XM_011529007.1:c.496+142_496+143del	XP_011527309.1:n.496+142_496+143del
XM_011529008.1:c.496+142_496+143del	XP_011527310.1:n.496+142_496+143del
XR_936612.1:n.729+142_729+143del
XM_024451971.1:c.169+142_169+143del	XP_024307739.1:n.169+142_169+143del
NM_003098.3:c.496+142_496+143del MANE Select	NP_003089.1:n.496+142_496+143del