Canonical Allele Identifier: CA8450442

Gene: MAP2K3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.21302241T>C , CM000679.2:g.21302241T>C	GRCh38
NC_000017.10:g.21205553T>C , CM000679.1:g.21205553T>C	GRCh37
NC_000017.9:g.21146146T>C	NCBI36
NG_028256.1:g.22586T>C
NG_028256.2:g.22586T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_145109.3:c.498T>C MANE Select	NP_659731.1:p.Leu166=
ENST00000342679.9:c.498T>C MANE Select	ENSP00000345083.4:p.Leu166=
NM_001316332.1:c.411T>C	NP_001303261.1:p.Leu137=
NM_001316332.2:c.411T>C	NP_001303261.1:p.Leu137=
NM_002756.4:c.411T>C	NP_002747.2:p.Leu137=
NM_145109.2:c.498T>C	NP_659731.1:p.Leu166=
ENST00000316920.10:c.411T>C	ENSP00000319139.6:p.Leu137=
ENST00000342679.8:c.498T>C	ENSP00000345083.4:p.Leu166=
ENST00000361818.9:c.411T>C	ENSP00000355081.5:p.Leu137=
ENST00000395491.6:c.*482T>C	ENSP00000378869.2:n.*482T>C
ENST00000496046.5:c.498T>C	ENSP00000464043.1:p.Leu166=
ENST00000526076.6:c.411T>C	ENSP00000434068.2:p.Leu137=
ENST00000613338.4:c.411T>C	ENSP00000478619.1:p.Leu137=
XM_005256723.2:c.411T>C	XP_005256780.1:p.Leu137=
XM_011523958.1:c.411T>C	XP_011522260.1:p.Leu137=
XM_011523958.2:c.411T>C	XP_011522260.1:p.Leu137=
XM_011523959.1:c.411T>C	XP_011522261.1:p.Leu137=
XM_011523959.2:c.411T>C	XP_011522261.1:p.Leu137=
XM_017024857.2:c.486T>C	XP_016880346.1:p.Leu162=
XM_017024858.1:c.411T>C	XP_016880347.1:p.Leu137=
XM_017024859.1:c.411T>C	XP_016880348.1:p.Leu137=