Canonical Allele Identifier: CA2530463970
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4094211dup , CM000681.2:g.4094211dup GRCh38
NC_000019.9:g.4094209dup , CM000681.1:g.4094209dup GRCh37
NC_000019.8:g.4045209dup NCBI36
NG_007996.1:g.34918dup , LRG_750:g.34918dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1531+242dup
ENST00000688002.1:n.3243+242dup
ENST00000688751.1:n.228+242dup
ENST00000689792.1:n.996+242dup
ENST00000262948.10:c.1092+242dup MANE Select ENSP00000262948.4:n.1092+242dup
ENST00000262948.9:c.1092+242dup ENSP00000262948.3:n.1092+242dup
ENST00000394867.8:c.801+242dup ENSP00000378336.1:n.801+242dup
ENST00000597263.5:n.277+242dup
ENST00000599021.1:c.202+242dup
ENST00000600584.5:n.2541+242dup
ENST00000601786.5:n.1393+242dup
NM_030662.3:c.1092+242dup , LRG_750t1:c.1092+242dup NP_109587.1:n.1092+242dup
XM_006722799.2:c.813+242dup XP_006722862.1:n.813+242dup
XM_011528133.1:c.522+242dup XP_011526435.1:n.522+242dup
NM_030662.4:c.1092+242dup MANE Select NP_109587.1:n.1092+242dup