Canonical Allele Identifier: CA8614135

Gene: MAP3K14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.45274220G>A , CM000679.2:g.45274220G>A	GRCh38
NC_000017.10:g.43351587G>A , CM000679.1:g.43351587G>A	GRCh37
NC_000017.9:g.40707370G>A	NCBI36
NG_033823.1:g.47829C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000344686.8:c.1455C>T MANE Select	ENSP00000478552.1:p.Gly485=
ENST00000617331.3:c.1455C>T	ENSP00000480974.3:p.Gly485=
ENST00000680632.1:c.303C>T	ENSP00000505027.1:p.Gly101=
ENST00000344686.6:c.1455C>T	ENSP00000478552.1:p.Gly485=
ENST00000376926.8:c.1455C>T	ENSP00000482657.1:p.Gly485=
NM_003954.4:c.1455C>T	NP_003945.2:p.Gly485=
XM_011525441.1:c.1455C>T	XP_011523743.1:p.Gly485=
XR_934591.1:n.1564C>T
NM_003954.5:c.1455C>T MANE Select	NP_003945.2:p.Gly485=
XM_011525441.2:c.1455C>T	XP_011523743.1:p.Gly485=