Canonical Allele Identifier: CA2319234289

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117451G= , CM000681.2:g.4117451G=	GRCh38
NC_000019.9:g.4117449G= , CM000681.1:g.4117449G=	GRCh37
NC_000019.8:g.4068449G=	NCBI36
NG_007996.1:g.11678C= , LRG_750:g.11678C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.710C=
ENST00000687128.1:n.710C=
ENST00000262948.10:c.271C= MANE Select	ENSP00000262948.4:p.His91=
ENST00000262948.9:c.271C=	ENSP00000262948.3:p.His91=
ENST00000394867.8:c.-21C=	ENSP00000378336.1:n.-21C=
ENST00000599345.1:n.468C=
NM_030662.3:c.271C= , LRG_750t1:c.271C=	NP_109587.1:p.His91=
XM_006722799.2:c.271C=	XP_006722862.1:p.His91=
XM_017026989.1:c.271C=	XP_016882478.1:p.His91=
XM_017026990.1:c.271C=	XP_016882479.1:p.His91=
XM_017026991.1:c.271C=	XP_016882480.1:p.His91=
NM_030662.4:c.271C= MANE Select	NP_109587.1:p.His91=