Canonical Allele Identifier: CA548089178

Gene: SPATA16

Linked Data

• dbSNP Id: rs1231551132
• gnomAD v2: 3-172798854-A-AT
• gnomAD v3: 3-173081064-A-AT
• gnomAD v4: 3-173081064-A-AT
• MyVariant Identifiers: chr3:g.172798854_172798855insT (hg19) ; chr3:g.173081064_173081065insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173081066dup , CM000665.2:g.173081066dup	GRCh38
NC_000003.11:g.172798856dup , CM000665.1:g.172798856dup	GRCh37
NC_000003.10:g.174281550dup	NCBI36
NG_021422.1:g.65204dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000351008.4:c.613-31971dup MANE Select	ENSP00000341765.3:n.613-31971dup
ENST00000351008.3:c.613-31971dup	ENSP00000341765.3:n.613-31971dup
NM_031955.5:c.613-31971dup	NP_114161.3:n.613-31971dup
XM_006713778.2:c.613-31971dup	XP_006713841.1:n.613-31971dup
XM_011513222.1:c.613-31971dup	XP_011511524.1:n.613-31971dup
XM_006713778.3:c.613-31971dup	XP_006713841.1:n.613-31971dup
XM_017007308.2:c.613-31971dup	XP_016862797.1:n.613-31971dup
NM_031955.6:c.613-31971dup MANE Select	NP_114161.3:n.613-31971dup