Canonical Allele Identifier: CA2319219790

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090702T= , CM000681.2:g.4090702T=	GRCh38
NC_000019.9:g.4090700T= , CM000681.1:g.4090700T=	GRCh37
NC_000019.8:g.4041700T=	NCBI36
NG_007996.1:g.38427A= , LRG_750:g.38427A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1538A=
ENST00000688002.1:n.3250A=
ENST00000688751.1:n.235A=
ENST00000689792.1:n.1003A=
ENST00000262948.10:c.1099A= MANE Select	ENSP00000262948.4:p.Thr367=
ENST00000262948.9:c.1099A=	ENSP00000262948.3:p.Thr367=
ENST00000394867.8:c.808A=	ENSP00000378336.1:p.Thr270=
ENST00000597263.5:n.284A=
ENST00000599021.1:c.209A=
ENST00000600584.5:n.2548A=
ENST00000601786.5:n.1400A=
NM_030662.3:c.1099A= , LRG_750t1:c.1099A=	NP_109587.1:p.Thr367=
XM_006722799.2:c.820A=	XP_006722862.1:p.Thr274=
XM_011528133.1:c.529A=	XP_011526435.1:p.Thr177=
NM_030662.4:c.1099A= MANE Select	NP_109587.1:p.Thr367=