Canonical Allele Identifier: CA2368281466

Gene: SPATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49906157_49906159delinsTCA , CM000682.2:g.49906157_49906159delinsTCA	GRCh38
NC_000020.10:g.48522694_48522696delinsTCA , CM000682.1:g.48522694_48522696delinsTCA	GRCh37
NC_000020.9:g.47956101_47956103delinsTCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289431.10:c.1023_1025delinsTGA MANE Select	ENSP00000289431.5:p.Ser341=
ENST00000289431.9:c.1023_1025delinsTGA	ENSP00000289431.5:p.Ser341=
ENST00000422556.1:c.1023_1025delinsTGA	ENSP00000416799.1:p.Ser341=
NM_001135773.1:c.1023_1025delinsTGA	NP_001129245.1:p.Ser341=
NM_006038.3:c.1023_1025delinsTGA	NP_006029.1:p.Ser341=
XM_006723894.1:c.1023_1025delinsTGA	XP_006723957.1:p.Ser341=
XM_011529116.1:c.1023_1025delinsTGA	XP_011527418.1:p.Ser341=
NM_006038.4:c.1023_1025delinsTGA MANE Select	NP_006029.1:p.Ser341=
NM_001135773.2:c.1023_1025delinsTGA	NP_001129245.1:p.Ser341=