Canonical Allele Identifier: CA8450705

Gene: MAP2K3

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.21312171C>T , CM000679.2:g.21312171C>T	GRCh38
NC_000017.10:g.21215483C>T , CM000679.1:g.21215483C>T	GRCh37
NG_028256.1:g.32516C>T
NG_028256.2:g.32516C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_145109.3:c.804C>T MANE Select	NP_659731.1:p.Tyr268=
ENST00000342679.9:c.804C>T MANE Select	ENSP00000345083.4:p.Tyr268=
NM_001316332.1:c.717C>T	NP_001303261.1:p.Tyr239=
NM_001316332.2:c.717C>T	NP_001303261.1:p.Tyr239=
NM_002756.4:c.717C>T	NP_002747.2:p.Tyr239=
NM_145109.2:c.804C>T	NP_659731.1:p.Tyr268=
ENST00000316920.10:c.717C>T	ENSP00000319139.6:p.Tyr239=
ENST00000342679.8:c.804C>T	ENSP00000345083.4:p.Tyr268=
ENST00000361818.9:c.717C>T	ENSP00000355081.5:p.Tyr239=
ENST00000395491.6:c.*788C>T	ENSP00000378869.2:n.*788C>T
ENST00000477540.1:n.485C>T
ENST00000496046.5:c.*230C>T	ENSP00000464043.1:n.*230C>T
ENST00000527123.1:c.30C>T	ENSP00000462178.1:p.Tyr10=
ENST00000613338.4:c.717C>T	ENSP00000478619.1:p.Tyr239=
XM_005256723.2:c.717C>T	XP_005256780.1:p.Tyr239=
XM_011523958.1:c.688-1321C>T	XP_011522260.1:n.688-1321C>T
XM_011523958.2:c.688-1321C>T	XP_011522260.1:n.688-1321C>T
XM_011523959.1:c.717C>T	XP_011522261.1:p.Tyr239=
XM_011523959.2:c.717C>T	XP_011522261.1:p.Tyr239=
XM_017024857.2:c.792C>T	XP_016880346.1:p.Tyr264=
XM_017024858.1:c.717C>T	XP_016880347.1:p.Tyr239=
XM_017024859.1:c.717C>T	XP_016880348.1:p.Tyr239=