Canonical Allele Identifier: CA8613775
Gene: MAP3K14 HGNC NCBI
MAP3K14-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45264738C>T , CM000679.2:g.45264738C>T GRCh38
NC_000017.10:g.43342105C>T , CM000679.1:g.43342105C>T GRCh37
NC_000017.9:g.40697888C>T NCBI36
NG_033823.1:g.57311G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000344686.8:c.2742G>A (MAP3K14) MANE Select ENSP00000478552.1:p.Glu914=
ENST00000586644.2:n.1679G>A (MAP3K14)
ENST00000617331.3:c.2742G>A (MAP3K14) ENSP00000480974.3:p.Glu914=
ENST00000680632.1:c.1796G>A (MAP3K14) ENSP00000505027.1:n.1796G>A
ENST00000344686.6:c.2742G>A (MAP3K14) ENSP00000478552.1:p.Glu914=
ENST00000376926.8:c.2742G>A (MAP3K14) ENSP00000482657.1:p.Glu914=
ENST00000592267.1:n.1549G>A (MAP3K14)
NM_003954.4:c.2742G>A (MAP3K14) NP_003945.2:p.Glu914=
NR_024434.2:n.80-2375C>T (MAP3K14-AS1)
NR_024435.2:n.265-1512C>T (MAP3K14-AS1)
NR_110324.1:n.265-2375C>T (MAP3K14-AS1)
NR_110325.1:n.260-2375C>T (MAP3K14-AS1)
NR_110326.1:n.164-2375C>T (MAP3K14-AS1)
XM_011525441.1:c.2742G>A (MAP3K14) XP_011523743.1:p.Glu914=
XR_934591.1:n.3057G>A (MAP3K14)
NM_003954.5:c.2742G>A (MAP3K14) MANE Select NP_003945.2:p.Glu914=
XM_011525441.2:c.2742G>A (MAP3K14) XP_011523743.1:p.Glu914=