Canonical Allele Identifier: CA2652477461

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33412227-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33412227T>C , CM000682.2:g.33412227T>C	GRCh38
NC_000020.10:g.32000033T>C , CM000682.1:g.32000033T>C	GRCh37
NC_000020.9:g.31463694T>C	NCBI36
NG_011622.1:g.36666A>G , LRG_332:g.36666A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.1040+69A>G MANE Select	ENSP00000217381.2:n.1040+69A>G
ENST00000217381.2:c.1040+69A>G	ENSP00000217381.2:n.1040+69A>G
NM_003098.2:c.1040+69A>G , LRG_332t1:c.1040+69A>G	NP_003089.1:n.1040+69A>G
XM_005260517.1:c.1040+69A>G	XP_005260574.1:n.1040+69A>G
XM_011529007.1:c.1040+69A>G	XP_011527309.1:n.1040+69A>G
XM_011529008.1:c.1040+69A>G	XP_011527310.1:n.1040+69A>G
XR_936612.1:n.1273+69A>G
XM_024451971.1:c.713+69A>G	XP_024307739.1:n.713+69A>G
NM_003098.3:c.1040+69A>G MANE Select	NP_003089.1:n.1040+69A>G