Canonical Allele Identifier: CA88219490

Gene: SPATA16

Linked Data

• dbSNP Id: rs35735356

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173081023dup , CM000665.2:g.173081023dup	GRCh38
NC_000003.11:g.172798813dup , CM000665.1:g.172798813dup	GRCh37
NC_000003.10:g.174281507dup	NCBI36
NG_021422.1:g.65248dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000351008.4:c.613-31927dup MANE Select	ENSP00000341765.3:n.613-31927dup
ENST00000351008.3:c.613-31927dup	ENSP00000341765.3:n.613-31927dup
NM_031955.5:c.613-31927dup	NP_114161.3:n.613-31927dup
XM_006713778.2:c.613-31927dup	XP_006713841.1:n.613-31927dup
XM_011513222.1:c.613-31927dup	XP_011511524.1:n.613-31927dup
XM_006713778.3:c.613-31927dup	XP_006713841.1:n.613-31927dup
XM_017007308.2:c.613-31927dup	XP_016862797.1:n.613-31927dup
NM_031955.6:c.613-31927dup MANE Select	NP_114161.3:n.613-31927dup