Canonical Allele Identifier: CA2652478037

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33438826-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438826A>G , CM000682.2:g.33438826A>G	GRCh38
NC_000020.10:g.32026632A>G , CM000682.1:g.32026632A>G	GRCh37
NC_000020.9:g.31490293A>G	NCBI36
NG_011622.1:g.10067T>C , LRG_332:g.10067T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+15T>C MANE Select	ENSP00000217381.2:n.496+15T>C
ENST00000217381.2:c.496+15T>C	ENSP00000217381.2:n.496+15T>C
NM_003098.2:c.496+15T>C , LRG_332t1:c.496+15T>C	NP_003089.1:n.496+15T>C
XM_005260517.1:c.496+15T>C	XP_005260574.1:n.496+15T>C
XM_011529007.1:c.496+15T>C	XP_011527309.1:n.496+15T>C
XM_011529008.1:c.496+15T>C	XP_011527310.1:n.496+15T>C
XR_936612.1:n.729+15T>C
XM_024451971.1:c.169+15T>C	XP_024307739.1:n.169+15T>C
NM_003098.3:c.496+15T>C MANE Select	NP_003089.1:n.496+15T>C