Canonical Allele Identifier: CA399864028

Gene: SPATA32 MAP3K14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45255542A>T , CM000679.2:g.45255542A>T	GRCh38
NC_000017.10:g.43332909A>T , CM000679.1:g.43332909A>T	GRCh37
NC_000017.9:g.40688692A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331780.5:c.640T>A (SPATA32) MANE Select	ENSP00000331532.4:p.Ser214Thr
ENST00000331780.4:c.640T>A (SPATA32)	ENSP00000331532.4:p.Ser214Thr
ENST00000586359.1:c.*1158T>A (SPATA32)	ENSP00000467344.1:n.*1158T>A
ENST00000588866.5:c.*547T>A (SPATA32)	ENSP00000467901.1:n.*547T>A
NM_152343.2:c.640T>A (SPATA32)	NP_689556.2:p.Ser214Thr
NR_024434.2:n.79+7539A>T (MAP3K14-AS1)
NR_110325.1:n.259+324A>T (MAP3K14-AS1)
NR_110326.1:n.163+324A>T (MAP3K14-AS1)
XM_011524300.1:c.577T>A (SPATA32)	XP_011522602.1:p.Ser193Thr
XM_011524301.1:c.577T>A (SPATA32)	XP_011522603.1:p.Ser193Thr
XR_934364.1:n.942T>A (SPATA32)
NM_152343.3:c.640T>A (SPATA32) MANE Select	NP_689556.2:p.Ser214Thr