Canonical Allele Identifier: CA2360752976

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438623_33438624delinsCA , CM000682.2:g.33438623_33438624delinsCA	GRCh38
NC_000020.10:g.32026429_32026430delinsCA , CM000682.1:g.32026429_32026430delinsCA	GRCh37
NC_000020.9:g.31490090_31490091delinsCA	NCBI36
NG_011622.1:g.10269_10270delinsTG , LRG_332:g.10269_10270delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+217_496+218delinsTG MANE Select	ENSP00000217381.2:n.496+217_496+218delinsTG
ENST00000217381.2:c.496+217_496+218delinsTG	ENSP00000217381.2:n.496+217_496+218delinsTG
NM_003098.2:c.496+217_496+218delinsTG , LRG_332t1:c.496+217_496+218delinsTG	NP_003089.1:n.496+217_496+218delinsTG
XM_005260517.1:c.496+217_496+218delinsTG	XP_005260574.1:n.496+217_496+218delinsTG
XM_011529007.1:c.496+217_496+218delinsTG	XP_011527309.1:n.496+217_496+218delinsTG
XM_011529008.1:c.496+217_496+218delinsTG	XP_011527310.1:n.496+217_496+218delinsTG
XR_936612.1:n.729+217_729+218delinsTG
XM_024451971.1:c.169+217_169+218delinsTG	XP_024307739.1:n.169+217_169+218delinsTG
NM_003098.3:c.496+217_496+218delinsTG MANE Select	NP_003089.1:n.496+217_496+218delinsTG