Canonical Allele Identifier: CA2652478028

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33438809-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33438809G>T , CM000682.2:g.33438809G>T	GRCh38
NC_000020.10:g.32026615G>T , CM000682.1:g.32026615G>T	GRCh37
NC_000020.9:g.31490276G>T	NCBI36
NG_011622.1:g.10084C>A , LRG_332:g.10084C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.496+32C>A MANE Select	ENSP00000217381.2:n.496+32C>A
ENST00000217381.2:c.496+32C>A	ENSP00000217381.2:n.496+32C>A
NM_003098.2:c.496+32C>A , LRG_332t1:c.496+32C>A	NP_003089.1:n.496+32C>A
XM_005260517.1:c.496+32C>A	XP_005260574.1:n.496+32C>A
XM_011529007.1:c.496+32C>A	XP_011527309.1:n.496+32C>A
XM_011529008.1:c.496+32C>A	XP_011527310.1:n.496+32C>A
XR_936612.1:n.729+32C>A
XM_024451971.1:c.169+32C>A	XP_024307739.1:n.169+32C>A
NM_003098.3:c.496+32C>A MANE Select	NP_003089.1:n.496+32C>A