Canonical Allele Identifier: CA398257021

Gene: MAP2K3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.21304526G>T , CM000679.2:g.21304526G>T	GRCh38
NC_000017.10:g.21207838G>T , CM000679.1:g.21207838G>T	GRCh37
NG_028256.1:g.24871G>T
NG_028256.2:g.24871G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342679.9:c.669G>T MANE Select	ENSP00000345083.4:p.Met223Ile
ENST00000316920.10:c.582G>T	ENSP00000319139.6:p.Met194Ile
ENST00000342679.8:c.669G>T	ENSP00000345083.4:p.Met223Ile
ENST00000361818.9:c.582G>T	ENSP00000355081.5:p.Met194Ile
ENST00000395491.6:c.*653G>T	ENSP00000378869.2:n.*653G>T
ENST00000496046.5:c.*95G>T	ENSP00000464043.1:n.*95G>T
ENST00000613338.4:c.582G>T	ENSP00000478619.1:p.Met194Ile
NM_001316332.1:c.582G>T	NP_001303261.1:p.Met194Ile
NM_002756.4:c.582G>T	NP_002747.2:p.Met194Ile
NM_145109.2:c.669G>T	NP_659731.1:p.Met223Ile
XM_005256723.2:c.582G>T	XP_005256780.1:p.Met194Ile
XM_011523958.1:c.582G>T	XP_011522260.1:p.Met194Ile
XM_011523959.1:c.582G>T	XP_011522261.1:p.Met194Ile
XM_011523958.2:c.582G>T	XP_011522260.1:p.Met194Ile
XM_011523959.2:c.582G>T	XP_011522261.1:p.Met194Ile
XM_017024857.2:c.657G>T	XP_016880346.1:p.Met219Ile
XM_017024858.1:c.582G>T	XP_016880347.1:p.Met194Ile
XM_017024859.1:c.582G>T	XP_016880348.1:p.Met194Ile
NM_001316332.2:c.582G>T	NP_001303261.1:p.Met194Ile
NM_145109.3:c.669G>T MANE Select	NP_659731.1:p.Met223Ile