Canonical Allele Identifier: CA2499336828

Gene: SPATA16

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.173081132_173081135del , CM000665.2:g.173081132_173081135del	GRCh38
NC_000003.11:g.172798922_172798925del , CM000665.1:g.172798922_172798925del	GRCh37
NC_000003.10:g.174281616_174281619del	NCBI36
NG_021422.1:g.65134_65137del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000351008.4:c.613-32041_613-32038del MANE Select	ENSP00000341765.3:n.613-32041_613-32038del
ENST00000351008.3:c.613-32041_613-32038del	ENSP00000341765.3:n.613-32041_613-32038del
NM_031955.5:c.613-32041_613-32038del	NP_114161.3:n.613-32041_613-32038del
XM_006713778.2:c.613-32041_613-32038del	XP_006713841.1:n.613-32041_613-32038del
XM_011513222.1:c.613-32041_613-32038del	XP_011511524.1:n.613-32041_613-32038del
XM_006713778.3:c.613-32041_613-32038del	XP_006713841.1:n.613-32041_613-32038del
XM_017007308.2:c.613-32041_613-32038del	XP_016862797.1:n.613-32041_613-32038del
NM_031955.6:c.613-32041_613-32038del MANE Select	NP_114161.3:n.613-32041_613-32038del