Canonical Allele Identifier: CA2319219778
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090668T= , CM000681.2:g.4090668T= GRCh38
NC_000019.9:g.4090666T= , CM000681.1:g.4090666T= GRCh37
NC_000019.8:g.4041666T= NCBI36
NG_007996.1:g.38461A= , LRG_750:g.38461A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1572A=
ENST00000688002.1:n.3284A=
ENST00000688751.1:n.269A=
ENST00000689792.1:n.1037A=
ENST00000262948.10:c.1133A= MANE Select ENSP00000262948.4:p.Asp378=
ENST00000262948.9:c.1133A= ENSP00000262948.3:p.Asp378=
ENST00000394867.8:c.842A= ENSP00000378336.1:p.Asp281=
ENST00000597263.5:n.318A=
ENST00000599021.1:c.243A=
ENST00000600584.5:n.2582A=
ENST00000601786.5:n.1434A=
NM_030662.3:c.1133A= , LRG_750t1:c.1133A= NP_109587.1:p.Asp378=
XM_006722799.2:c.854A= XP_006722862.1:p.Asp285=
XM_011528133.1:c.563A= XP_011526435.1:p.Asp188=
NM_030662.4:c.1133A= MANE Select NP_109587.1:p.Asp378=