Canonical Allele Identifier: CA2838532060

Gene: MAP2K3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.21301070C>A , CM000679.2:g.21301070C>A	GRCh38
NC_000017.10:g.21204382C>A , CM000679.1:g.21204382C>A	GRCh37
NC_000017.9:g.21144975C>A	NCBI36
NG_028256.1:g.21415C>A
NG_028256.2:g.21415C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342679.9:c.399+77C>A MANE Select	ENSP00000345083.4:n.399+77C>A
ENST00000316920.10:c.312+77C>A	ENSP00000319139.6:n.312+77C>A
ENST00000342679.8:c.399+77C>A	ENSP00000345083.4:n.399+77C>A
ENST00000361818.9:c.312+77C>A	ENSP00000355081.5:n.312+77C>A
ENST00000395491.6:c.*383+77C>A	ENSP00000378869.2:n.*383+77C>A
ENST00000496046.5:c.399+77C>A	ENSP00000464043.1:n.399+77C>A
ENST00000526076.6:c.312+77C>A	ENSP00000434068.2:n.312+77C>A
ENST00000613338.4:c.312+77C>A	ENSP00000478619.1:n.312+77C>A
NM_001316332.1:c.312+77C>A	NP_001303261.1:n.312+77C>A
NM_002756.4:c.312+77C>A	NP_002747.2:n.312+77C>A
NM_145109.2:c.399+77C>A	NP_659731.1:n.399+77C>A
XM_005256723.2:c.312+77C>A	XP_005256780.1:n.312+77C>A
XM_011523958.1:c.312+77C>A	XP_011522260.1:n.312+77C>A
XM_011523959.1:c.312+77C>A	XP_011522261.1:n.312+77C>A
XM_011523958.2:c.312+77C>A	XP_011522260.1:n.312+77C>A
XM_011523959.2:c.312+77C>A	XP_011522261.1:n.312+77C>A
XM_017024857.2:c.387+77C>A	XP_016880346.1:n.387+77C>A
XM_017024858.1:c.312+77C>A	XP_016880347.1:n.312+77C>A
XM_017024859.1:c.312+77C>A	XP_016880348.1:n.312+77C>A
NM_001316332.2:c.312+77C>A	NP_001303261.1:n.312+77C>A
NM_145109.3:c.399+77C>A MANE Select	NP_659731.1:n.399+77C>A