Canonical Allele Identifier: CA8613700

Gene: SPATA32 MAP3K14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45257171A>G , CM000679.2:g.45257171A>G	GRCh38
NC_000017.10:g.43334538A>G , CM000679.1:g.43334538A>G	GRCh37
NC_000017.9:g.40690321A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331780.5:c.50T>C (SPATA32) MANE Select	ENSP00000331532.4:p.Val17Ala
ENST00000331780.4:c.50T>C (SPATA32)	ENSP00000331532.4:p.Val17Ala
ENST00000586359.1:c.*568T>C (SPATA32)	ENSP00000467344.1:n.*568T>C
ENST00000588866.5:c.50T>C (SPATA32)	ENSP00000467901.1:p.Val17Ala
NM_152343.2:c.50T>C (SPATA32)	NP_689556.2:p.Val17Ala
NR_024434.2:n.79+9168A>G (MAP3K14-AS1)
NR_110325.1:n.259+1953A>G (MAP3K14-AS1)
NR_110326.1:n.163+1953A>G (MAP3K14-AS1)
XM_011524300.1:c.-14T>C (SPATA32)	XP_011522602.1:n.-14T>C
XM_011524301.1:c.-14T>C (SPATA32)	XP_011522603.1:n.-14T>C
XR_934364.1:n.331T>C (SPATA32)
NM_152343.3:c.50T>C (SPATA32) MANE Select	NP_689556.2:p.Val17Ala