Canonical Allele Identifier: CA2368281180

Gene: SPATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49905550_49905552delinsTAC , CM000682.2:g.49905550_49905552delinsTAC	GRCh38
NC_000020.10:g.48522087_48522089delinsTAC , CM000682.1:g.48522087_48522089delinsTAC	GRCh37
NC_000020.9:g.47955494_47955496delinsTAC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289431.10:c.*67_*69delinsGTA MANE Select	ENSP00000289431.5:n.*67_*69delinsGTA
ENST00000289431.9:c.*67_*69delinsGTA	ENSP00000289431.5:n.*67_*69delinsGTA
ENST00000422556.1:c.*67_*69delinsGTA	ENSP00000416799.1:n.*67_*69delinsGTA
NM_001135773.1:c.*67_*69delinsGTA	NP_001129245.1:n.*67_*69delinsGTA
NM_006038.3:c.*67_*69delinsGTA	NP_006029.1:n.*67_*69delinsGTA
XM_006723894.1:c.*67_*69delinsGTA	XP_006723957.1:n.*67_*69delinsGTA
XM_011529116.1:c.*67_*69delinsGTA	XP_011527418.1:n.*67_*69delinsGTA
NM_006038.4:c.*67_*69delinsGTA MANE Select	NP_006029.1:n.*67_*69delinsGTA
NM_001135773.2:c.*67_*69delinsGTA	NP_001129245.1:n.*67_*69delinsGTA