Canonical Allele Identifier: CA8614025

Gene: MAP3K14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45271045T>G , CM000679.2:g.45271045T>G	GRCh38
NC_000017.10:g.43348412T>G , CM000679.1:g.43348412T>G	GRCh37
NC_000017.9:g.40704195T>G	NCBI36
NG_033823.1:g.51004A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_003954.5:c.1821+13A>C MANE Select	NP_003945.2:n.1821+13A>C
ENST00000344686.8:c.1821+13A>C MANE Select	ENSP00000478552.1:n.1821+13A>C
NM_003954.4:c.1821+13A>C	NP_003945.2:n.1821+13A>C
ENST00000344686.6:c.1821+13A>C	ENSP00000478552.1:n.1821+13A>C
ENST00000376926.8:c.1821+13A>C	ENSP00000482657.1:n.1821+13A>C
ENST00000586644.1:n.277A>C
ENST00000586644.2:n.277A>C
ENST00000592267.1:n.628+13A>C
ENST00000617331.3:c.1821+13A>C	ENSP00000480974.3:n.1821+13A>C
ENST00000680632.1:c.682A>C	ENSP00000505027.1:p.Thr228Pro
XM_011525441.1:c.1821+13A>C	XP_011523743.1:n.1821+13A>C
XM_011525441.2:c.1821+13A>C	XP_011523743.1:n.1821+13A>C
XR_934591.1:n.1943A>C