Canonical Allele Identifier: CA8613760

Gene: MAP3K14 MAP3K14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45264654C>T , CM000679.2:g.45264654C>T	GRCh38
NC_000017.10:g.43342021C>T , CM000679.1:g.43342021C>T	GRCh37
NC_000017.9:g.40697804C>T	NCBI36
NG_033823.1:g.57395G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.2826G>A (MAP3K14) MANE Select	ENSP00000478552.1:p.Gln942=
ENST00000586644.2:n.1763G>A (MAP3K14)
ENST00000617331.3:c.2826G>A (MAP3K14)	ENSP00000480974.3:p.Gln942=
ENST00000680632.1:c.1880G>A (MAP3K14)	ENSP00000505027.1:n.1880G>A
ENST00000344686.6:c.2826G>A (MAP3K14)	ENSP00000478552.1:p.Gln942=
ENST00000376926.8:c.2826G>A (MAP3K14)	ENSP00000482657.1:p.Gln942=
ENST00000592267.1:n.1633G>A (MAP3K14)
NM_003954.4:c.2826G>A (MAP3K14)	NP_003945.2:p.Gln942=
NR_024434.2:n.80-2459C>T (MAP3K14-AS1)
NR_024435.2:n.265-1596C>T (MAP3K14-AS1)
NR_110324.1:n.264+2311C>T (MAP3K14-AS1)
NR_110325.1:n.260-2459C>T (MAP3K14-AS1)
NR_110326.1:n.164-2459C>T (MAP3K14-AS1)
XM_011525441.1:c.2826G>A (MAP3K14)	XP_011523743.1:p.Gln942=
XR_934591.1:n.3141G>A (MAP3K14)
NM_003954.5:c.2826G>A (MAP3K14) MANE Select	NP_003945.2:p.Gln942=
XM_011525441.2:c.2826G>A (MAP3K14)	XP_011523743.1:p.Gln942=