Canonical Allele Identifier: CA8613871

Gene: MAP3K14 MAP3K14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45266691C>T , CM000679.2:g.45266691C>T	GRCh38
NC_000017.10:g.43344058C>T , CM000679.1:g.43344058C>T	GRCh37
NC_000017.9:g.40699841C>T	NCBI36
NG_033823.1:g.55358G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.2434-10G>A (MAP3K14) MANE Select	ENSP00000478552.1:n.2434-10G>A
ENST00000586644.2:n.1371-10G>A (MAP3K14)
ENST00000617331.3:c.2434-10G>A (MAP3K14)	ENSP00000480974.3:n.2434-10G>A
ENST00000680632.1:c.1488-10G>A (MAP3K14)	ENSP00000505027.1:n.1488-10G>A
ENST00000344686.6:c.2434-10G>A (MAP3K14)	ENSP00000478552.1:n.2434-10G>A
ENST00000376926.8:c.2434-10G>A (MAP3K14)	ENSP00000482657.1:n.2434-10G>A
ENST00000592267.1:n.1241-10G>A (MAP3K14)
NM_003954.4:c.2434-10G>A (MAP3K14)	NP_003945.2:n.2434-10G>A
NR_024434.2:n.80-422C>T (MAP3K14-AS1)
NR_024435.2:n.533+173C>T (MAP3K14-AS1)
NR_110324.1:n.265-422C>T (MAP3K14-AS1)
NR_110325.1:n.260-422C>T (MAP3K14-AS1)
NR_110326.1:n.164-422C>T (MAP3K14-AS1)
XM_011525441.1:c.2434-10G>A (MAP3K14)	XP_011523743.1:n.2434-10G>A
XR_934591.1:n.2749-10G>A (MAP3K14)
NM_003954.5:c.2434-10G>A (MAP3K14) MANE Select	NP_003945.2:n.2434-10G>A
XM_011525441.2:c.2434-10G>A (MAP3K14)	XP_011523743.1:n.2434-10G>A