Canonical Allele Identifier: CA2368281468

Gene: SPATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49906161A= , CM000682.2:g.49906161A=	GRCh38
NC_000020.10:g.48522698A= , CM000682.1:g.48522698A=	GRCh37
NC_000020.9:g.47956105A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289431.10:c.1021T= MANE Select	ENSP00000289431.5:p.Ser341=
ENST00000289431.9:c.1021T=	ENSP00000289431.5:p.Ser341=
ENST00000422556.1:c.1021T=	ENSP00000416799.1:p.Ser341=
NM_001135773.1:c.1021T=	NP_001129245.1:p.Ser341=
NM_006038.3:c.1021T=	NP_006029.1:p.Ser341=
XM_006723894.1:c.1021T=	XP_006723957.1:p.Ser341=
XM_011529116.1:c.1021T=	XP_011527418.1:p.Ser341=
NM_006038.4:c.1021T= MANE Select	NP_006029.1:p.Ser341=
NM_001135773.2:c.1021T=	NP_001129245.1:p.Ser341=