Canonical Allele Identifier: CA2368281184

Gene: SPATA2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.49905555_49905556delinsCT , CM000682.2:g.49905555_49905556delinsCT	GRCh38
NC_000020.10:g.48522092_48522093delinsCT , CM000682.1:g.48522092_48522093delinsCT	GRCh37
NC_000020.9:g.47955499_47955500delinsCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000289431.10:c.*63_*64delinsAG MANE Select	ENSP00000289431.5:n.*63_*64delinsAG
ENST00000289431.9:c.*63_*64delinsAG	ENSP00000289431.5:n.*63_*64delinsAG
ENST00000422556.1:c.*63_*64delinsAG	ENSP00000416799.1:n.*63_*64delinsAG
NM_001135773.1:c.*63_*64delinsAG	NP_001129245.1:n.*63_*64delinsAG
NM_006038.3:c.*63_*64delinsAG	NP_006029.1:n.*63_*64delinsAG
XM_006723894.1:c.*63_*64delinsAG	XP_006723957.1:n.*63_*64delinsAG
XM_011529116.1:c.*63_*64delinsAG	XP_011527418.1:n.*63_*64delinsAG
NM_006038.4:c.*63_*64delinsAG MANE Select	NP_006029.1:n.*63_*64delinsAG
NM_001135773.2:c.*63_*64delinsAG	NP_001129245.1:n.*63_*64delinsAG