Canonical Allele Identifier: CA399866172

Gene: SPATA32 MAP3K14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45256025C>G , CM000679.2:g.45256025C>G	GRCh38
NC_000017.10:g.43333392C>G , CM000679.1:g.43333392C>G	GRCh37
NC_000017.9:g.40689175C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331780.5:c.157G>C (SPATA32) MANE Select	ENSP00000331532.4:p.Asp53His
ENST00000331780.4:c.157G>C (SPATA32)	ENSP00000331532.4:p.Asp53His
ENST00000586359.1:c.*675G>C (SPATA32)	ENSP00000467344.1:n.*675G>C
ENST00000588866.5:c.*64G>C (SPATA32)	ENSP00000467901.1:n.*64G>C
NM_152343.2:c.157G>C (SPATA32)	NP_689556.2:p.Asp53His
NR_024434.2:n.79+8022C>G (MAP3K14-AS1)
NR_110325.1:n.259+807C>G (MAP3K14-AS1)
NR_110326.1:n.163+807C>G (MAP3K14-AS1)
XM_011524300.1:c.94G>C (SPATA32)	XP_011522602.1:p.Asp32His
XM_011524301.1:c.94G>C (SPATA32)	XP_011522603.1:p.Asp32His
XR_934364.1:n.459G>C (SPATA32)
NM_152343.3:c.157G>C (SPATA32) MANE Select	NP_689556.2:p.Asp53His