Canonical Allele Identifier: CA2577372552

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33412230-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33412234del , CM000682.2:g.33412234del	GRCh38
NC_000020.10:g.32000040del , CM000682.1:g.32000040del	GRCh37
NC_000020.9:g.31463701del	NCBI36
NG_011622.1:g.36662del , LRG_332:g.36662del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.1040+65del MANE Select	ENSP00000217381.2:n.1040+65del
ENST00000217381.2:c.1040+65del	ENSP00000217381.2:n.1040+65del
NM_003098.2:c.1040+65del , LRG_332t1:c.1040+65del	NP_003089.1:n.1040+65del
XM_005260517.1:c.1040+65del	XP_005260574.1:n.1040+65del
XM_011529007.1:c.1040+65del	XP_011527309.1:n.1040+65del
XM_011529008.1:c.1040+65del	XP_011527310.1:n.1040+65del
XR_936612.1:n.1273+65del
XM_024451971.1:c.713+65del	XP_024307739.1:n.713+65del
NM_003098.3:c.1040+65del MANE Select	NP_003089.1:n.1040+65del