Canonical Allele Identifier: CA2360752960

Gene: SNTA1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438593_33438594delinsTC , CM000682.2:g.33438593_33438594delinsTC	GRCh38
NC_000020.10:g.32026399_32026400delinsTC , CM000682.1:g.32026399_32026400delinsTC	GRCh37
NC_000020.9:g.31490060_31490061delinsTC	NCBI36
NG_011622.1:g.10299_10300delinsGA , LRG_332:g.10299_10300delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+247_496+248delinsGA MANE Select	ENSP00000217381.2:n.496+247_496+248delinsGA
ENST00000217381.2:c.496+247_496+248delinsGA	ENSP00000217381.2:n.496+247_496+248delinsGA
NM_003098.2:c.496+247_496+248delinsGA , LRG_332t1:c.496+247_496+248delinsGA	NP_003089.1:n.496+247_496+248delinsGA
XM_005260517.1:c.496+247_496+248delinsGA	XP_005260574.1:n.496+247_496+248delinsGA
XM_011529007.1:c.496+247_496+248delinsGA	XP_011527309.1:n.496+247_496+248delinsGA
XM_011529008.1:c.496+247_496+248delinsGA	XP_011527310.1:n.496+247_496+248delinsGA
XR_936612.1:n.729+247_729+248delinsGA
XM_024451971.1:c.169+247_169+248delinsGA	XP_024307739.1:n.169+247_169+248delinsGA
NM_003098.3:c.496+247_496+248delinsGA MANE Select	NP_003089.1:n.496+247_496+248delinsGA