Canonical Allele Identifier: CA2261779202

Gene: MAP3K14 MAP3K14-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45267333A= , CM000679.2:g.45267333A=	GRCh38
NC_000017.10:g.43344700A= , CM000679.1:g.43344700A=	GRCh37
NC_000017.9:g.40700483A=	NCBI36
NG_033823.1:g.54716T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000344686.8:c.2326+73T= (MAP3K14) MANE Select	ENSP00000478552.1:n.2326+73T=
ENST00000586644.2:n.1263+73T= (MAP3K14)
ENST00000617331.3:c.2326+73T= (MAP3K14)	ENSP00000480974.3:n.2326+73T=
ENST00000680632.1:c.1380+73T= (MAP3K14)	ENSP00000505027.1:n.1380+73T=
ENST00000344686.6:c.2326+73T= (MAP3K14)	ENSP00000478552.1:n.2326+73T=
ENST00000376926.8:c.2326+73T= (MAP3K14)	ENSP00000482657.1:n.2326+73T=
ENST00000592267.1:n.1133+73T= (MAP3K14)
NM_003954.4:c.2326+73T= (MAP3K14)	NP_003945.2:n.2326+73T=
NR_024434.2:n.295+5A= (MAP3K14-AS1)
NR_024435.2:n.749+5A= (MAP3K14-AS1)
NR_110324.1:n.480+5A= (MAP3K14-AS1)
NR_110325.1:n.475+5A= (MAP3K14-AS1)
NR_110326.1:n.379+5A= (MAP3K14-AS1)
XM_011525441.1:c.2326+73T= (MAP3K14)	XP_011523743.1:n.2326+73T=
XR_934591.1:n.2641+73T= (MAP3K14)
NM_003954.5:c.2326+73T= (MAP3K14) MANE Select	NP_003945.2:n.2326+73T=
XM_011525441.2:c.2326+73T= (MAP3K14)	XP_011523743.1:n.2326+73T=