Canonical Allele Identifier: CA658132616

Gene: SPATA2

Linked Data

• COSMIC: COSN19727926

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49905574dup , CM000682.2:g.49905574dup	GRCh38
NC_000020.10:g.48522111dup , CM000682.1:g.48522111dup	GRCh37
NC_000020.9:g.47955518dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289431.10:c.*47dup MANE Select	ENSP00000289431.5:n.*47dup
ENST00000289431.9:c.*47dup	ENSP00000289431.5:n.*47dup
ENST00000422556.1:c.*47dup	ENSP00000416799.1:n.*47dup
NM_001135773.1:c.*47dup	NP_001129245.1:n.*47dup
NM_006038.3:c.*47dup	NP_006029.1:n.*47dup
XM_006723894.1:c.*47dup	XP_006723957.1:n.*47dup
XM_011529116.1:c.*47dup	XP_011527418.1:n.*47dup
NM_006038.4:c.*47dup MANE Select	NP_006029.1:n.*47dup
NM_001135773.2:c.*47dup	NP_001129245.1:n.*47dup