Canonical Allele Identifier: CA2813356262

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094299A>G , CM000681.2:g.4094299A>G	GRCh38
NC_000019.9:g.4094297A>G , CM000681.1:g.4094297A>G	GRCh37
NC_000019.8:g.4045297A>G	NCBI36
NG_007996.1:g.34830T>C , LRG_750:g.34830T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1531+154T>C
ENST00000688002.1:n.3243+154T>C
ENST00000688751.1:n.228+154T>C
ENST00000689792.1:n.996+154T>C
ENST00000262948.10:c.1092+154T>C MANE Select	ENSP00000262948.4:n.1092+154T>C
ENST00000262948.9:c.1092+154T>C	ENSP00000262948.3:n.1092+154T>C
ENST00000394867.8:c.801+154T>C	ENSP00000378336.1:n.801+154T>C
ENST00000597263.5:n.277+154T>C
ENST00000599021.1:c.202+154T>C
ENST00000600584.5:n.2541+154T>C
ENST00000601786.5:n.1393+154T>C
NM_030662.3:c.1092+154T>C , LRG_750t1:c.1092+154T>C	NP_109587.1:n.1092+154T>C
XM_006722799.2:c.813+154T>C	XP_006722862.1:n.813+154T>C
XM_011528133.1:c.522+154T>C	XP_011526435.1:n.522+154T>C
NM_030662.4:c.1092+154T>C MANE Select	NP_109587.1:n.1092+154T>C