Canonical Allele Identifier: CA291053677

Gene: MAP3K14 MAP3K14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45267158C>T , CM000679.2:g.45267158C>T	GRCh38
NC_000017.10:g.43344525C>T , CM000679.1:g.43344525C>T	GRCh37
NC_000017.9:g.40700308C>T	NCBI36
NG_033823.1:g.54891G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_003954.5:c.2367G>A (MAP3K14) MANE Select	NP_003945.2:p.Glu789=
ENST00000344686.8:c.2367G>A (MAP3K14) MANE Select	ENSP00000478552.1:p.Glu789=
NM_003954.4:c.2367G>A (MAP3K14)	NP_003945.2:p.Glu789=
NR_024434.2:n.125C>T (MAP3K14-AS1)
NR_024435.2:n.579C>T (MAP3K14-AS1)
NR_110324.1:n.310C>T (MAP3K14-AS1)
NR_110325.1:n.305C>T (MAP3K14-AS1)
NR_110326.1:n.209C>T (MAP3K14-AS1)
ENST00000344686.6:c.2367G>A (MAP3K14)	ENSP00000478552.1:p.Glu789=
ENST00000376926.8:c.2367G>A (MAP3K14)	ENSP00000482657.1:p.Glu789=
ENST00000586644.2:n.1304G>A (MAP3K14)
ENST00000592267.1:n.1174G>A (MAP3K14)
ENST00000617331.3:c.2367G>A (MAP3K14)	ENSP00000480974.3:p.Glu789=
ENST00000680632.1:c.1421G>A (MAP3K14)	ENSP00000505027.1:n.1421G>A
XM_011525441.1:c.2367G>A (MAP3K14)	XP_011523743.1:p.Glu789=
XM_011525441.2:c.2367G>A (MAP3K14)	XP_011523743.1:p.Glu789=
XR_934591.1:n.2682G>A (MAP3K14)