Canonical Allele Identifier: CA8613786

Gene: MAP3K14 MAP3K14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45264774G>C , CM000679.2:g.45264774G>C	GRCh38
NC_000017.10:g.43342141G>C , CM000679.1:g.43342141G>C	GRCh37
NC_000017.9:g.40697924G>C	NCBI36
NG_033823.1:g.57275C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_003954.5:c.2706C>G (MAP3K14) MANE Select	NP_003945.2:p.Val902=
ENST00000344686.8:c.2706C>G (MAP3K14) MANE Select	ENSP00000478552.1:p.Val902=
NM_003954.4:c.2706C>G (MAP3K14)	NP_003945.2:p.Val902=
NR_024434.2:n.80-2339G>C (MAP3K14-AS1)
NR_024435.2:n.265-1476G>C (MAP3K14-AS1)
NR_110324.1:n.265-2339G>C (MAP3K14-AS1)
NR_110325.1:n.260-2339G>C (MAP3K14-AS1)
NR_110326.1:n.164-2339G>C (MAP3K14-AS1)
ENST00000344686.6:c.2706C>G (MAP3K14)	ENSP00000478552.1:p.Val902=
ENST00000376926.8:c.2706C>G (MAP3K14)	ENSP00000482657.1:p.Val902=
ENST00000586644.2:n.1643C>G (MAP3K14)
ENST00000592267.1:n.1513C>G (MAP3K14)
ENST00000617331.3:c.2706C>G (MAP3K14)	ENSP00000480974.3:p.Val902=
ENST00000680632.1:c.1760C>G (MAP3K14)	ENSP00000505027.1:n.1760C>G
XM_011525441.1:c.2706C>G (MAP3K14)	XP_011523743.1:p.Val902=
XM_011525441.2:c.2706C>G (MAP3K14)	XP_011523743.1:p.Val902=
XR_934591.1:n.3021C>G (MAP3K14)