Canonical Allele Identifier: CA8613761

Gene: MAP3K14 MAP3K14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45264660A>G , CM000679.2:g.45264660A>G	GRCh38
NC_000017.10:g.43342027A>G , CM000679.1:g.43342027A>G	GRCh37
NC_000017.9:g.40697810A>G	NCBI36
NG_033823.1:g.57389T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.2820T>C (MAP3K14) MANE Select	ENSP00000478552.1:p.His940=
ENST00000586644.2:n.1757T>C (MAP3K14)
ENST00000617331.3:c.2820T>C (MAP3K14)	ENSP00000480974.3:p.His940=
ENST00000680632.1:c.1874T>C (MAP3K14)	ENSP00000505027.1:n.1874T>C
ENST00000344686.6:c.2820T>C (MAP3K14)	ENSP00000478552.1:p.His940=
ENST00000376926.8:c.2820T>C (MAP3K14)	ENSP00000482657.1:p.His940=
ENST00000592267.1:n.1627T>C (MAP3K14)
NM_003954.4:c.2820T>C (MAP3K14)	NP_003945.2:p.His940=
NR_024434.2:n.80-2453A>G (MAP3K14-AS1)
NR_024435.2:n.265-1590A>G (MAP3K14-AS1)
NR_110324.1:n.264+2317A>G (MAP3K14-AS1)
NR_110325.1:n.260-2453A>G (MAP3K14-AS1)
NR_110326.1:n.164-2453A>G (MAP3K14-AS1)
XM_011525441.1:c.2820T>C (MAP3K14)	XP_011523743.1:p.His940=
XR_934591.1:n.3135T>C (MAP3K14)
NM_003954.5:c.2820T>C (MAP3K14) MANE Select	NP_003945.2:p.His940=
XM_011525441.2:c.2820T>C (MAP3K14)	XP_011523743.1:p.His940=