Canonical Allele Identifier: CA1056448692

Gene: SPATA16

Linked Data

• dbSNP Id: rs1736908717
• gnomAD v3: 3-173080964-GC-G
• gnomAD v4: 3-173080964-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173080965del , CM000665.2:g.173080965del	GRCh38
NC_000003.11:g.172798755del , CM000665.1:g.172798755del	GRCh37
NC_000003.10:g.174281449del	NCBI36
NG_021422.1:g.65304del

Transcript Alleles

HGVS	Amino-acid change
ENST00000351008.4:c.613-31871del MANE Select	ENSP00000341765.3:n.613-31871del
ENST00000351008.3:c.613-31871del	ENSP00000341765.3:n.613-31871del
NM_031955.5:c.613-31871del	NP_114161.3:n.613-31871del
XM_006713778.2:c.613-31871del	XP_006713841.1:n.613-31871del
XM_011513222.1:c.613-31871del	XP_011511524.1:n.613-31871del
XM_006713778.3:c.613-31871del	XP_006713841.1:n.613-31871del
XM_017007308.2:c.613-31871del	XP_016862797.1:n.613-31871del
NM_031955.6:c.613-31871del MANE Select	NP_114161.3:n.613-31871del