Canonical Allele Identifier: CA2652478041

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33438935-G-GGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438936_33438937insAAG , CM000682.2:g.33438936_33438937insAAG	GRCh38
NC_000020.10:g.32026742_32026743insAAG , CM000682.1:g.32026742_32026743insAAG	GRCh37
NC_000020.9:g.31490403_31490404insAAG	NCBI36
NG_011622.1:g.9957_9958insTTC , LRG_332:g.9957_9958insTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.401_402insTTC MANE Select	ENSP00000217381.2:p.Ala134_Ile135insSer
ENST00000217381.2:c.401_402insTTC	ENSP00000217381.2:p.Ala134_Ile135insSer
NM_003098.2:c.401_402insTTC , LRG_332t1:c.401_402insTTC	NP_003089.1:p.Ala134_Ile135insSer
XM_005260517.1:c.401_402insTTC	XP_005260574.1:p.Ala134_Ile135insSer
XM_011529007.1:c.401_402insTTC	XP_011527309.1:p.Ala134_Ile135insSer
XM_011529008.1:c.401_402insTTC	XP_011527310.1:p.Ala134_Ile135insSer
XR_936612.1:n.634_635insTTC
XM_024451971.1:c.74_75insTTC	XP_024307739.1:p.Ala25_Ile26insSer
NM_003098.3:c.401_402insTTC MANE Select	NP_003089.1:p.Ala134_Ile135insSer