Canonical Allele Identifier: CA2368281315

Gene: SPATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49905842T= , CM000682.2:g.49905842T=	GRCh38
NC_000020.10:g.48522379T= , CM000682.1:g.48522379T=	GRCh37
NC_000020.9:g.47955786T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289431.10:c.1340A= MANE Select	ENSP00000289431.5:p.His447=
ENST00000289431.9:c.1340A=	ENSP00000289431.5:p.His447=
ENST00000422556.1:c.1340A=	ENSP00000416799.1:p.His447=
NM_001135773.1:c.1340A=	NP_001129245.1:p.His447=
NM_006038.3:c.1340A=	NP_006029.1:p.His447=
XM_006723894.1:c.1340A=	XP_006723957.1:p.His447=
XM_011529116.1:c.1340A=	XP_011527418.1:p.His447=
NM_006038.4:c.1340A= MANE Select	NP_006029.1:p.His447=
NM_001135773.2:c.1340A=	NP_001129245.1:p.His447=