Canonical Allele Identifier: CA2319219788
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090692T= , CM000681.2:g.4090692T= GRCh38
NC_000019.9:g.4090690T= , CM000681.1:g.4090690T= GRCh37
NC_000019.8:g.4041690T= NCBI36
NG_007996.1:g.38437A= , LRG_750:g.38437A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1548A=
ENST00000688002.1:n.3260A=
ENST00000688751.1:n.245A=
ENST00000689792.1:n.1013A=
ENST00000262948.10:c.1109A= MANE Select ENSP00000262948.4:p.Lys370=
ENST00000262948.9:c.1109A= ENSP00000262948.3:p.Lys370=
ENST00000394867.8:c.818A= ENSP00000378336.1:p.Lys273=
ENST00000597263.5:n.294A=
ENST00000599021.1:c.219A=
ENST00000600584.5:n.2558A=
ENST00000601786.5:n.1410A=
NM_030662.3:c.1109A= , LRG_750t1:c.1109A= NP_109587.1:p.Lys370=
XM_006722799.2:c.830A= XP_006722862.1:p.Lys277=
XM_011528133.1:c.539A= XP_011526435.1:p.Lys180=
NM_030662.4:c.1109A= MANE Select NP_109587.1:p.Lys370=