Canonical Allele Identifier: CA2652478046

Gene: SNTA1

Linked Data

• gnomAD v4: 20-33439036-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33439037dup , CM000682.2:g.33439037dup	GRCh38
NC_000020.10:g.32026843dup , CM000682.1:g.32026843dup	GRCh37
NC_000020.9:g.31490504dup	NCBI36
NG_011622.1:g.9856dup , LRG_332:g.9856dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000217381.3:c.311-11dup MANE Select	ENSP00000217381.2:n.311-11dup
ENST00000217381.2:c.311-11dup	ENSP00000217381.2:n.311-11dup
NM_003098.2:c.311-11dup , LRG_332t1:c.311-11dup	NP_003089.1:n.311-11dup
XM_005260517.1:c.311-11dup	XP_005260574.1:n.311-11dup
XM_011529007.1:c.311-11dup	XP_011527309.1:n.311-11dup
XM_011529008.1:c.311-11dup	XP_011527310.1:n.311-11dup
XR_936612.1:n.544-11dup
XM_024451971.1:c.-17-11dup	XP_024307739.1:n.-17-11dup
NM_003098.3:c.311-11dup MANE Select	NP_003089.1:n.311-11dup