Canonical Allele Identifier: CA2319234212
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4117346T= , CM000681.2:g.4117346T= GRCh38
NC_000019.9:g.4117344T= , CM000681.1:g.4117344T= GRCh37
NC_000019.8:g.4068344T= NCBI36
NG_007996.1:g.11783A= , LRG_750:g.11783A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.742+73A=
ENST00000687128.1:n.742+73A=
ENST00000262948.10:c.303+73A= MANE Select ENSP00000262948.4:n.303+73A=
ENST00000262948.9:c.303+73A= ENSP00000262948.3:n.303+73A=
ENST00000394867.8:c.12+73A= ENSP00000378336.1:n.12+73A=
ENST00000599345.1:n.500+73A=
NM_030662.3:c.303+73A= , LRG_750t1:c.303+73A= NP_109587.1:n.303+73A=
XM_006722799.2:c.303+73A= XP_006722862.1:n.303+73A=
XM_017026989.1:c.303+73A= XP_016882478.1:n.303+73A=
XM_017026990.1:c.303+73A= XP_016882479.1:n.303+73A=
XM_017026991.1:c.303+73A= XP_016882480.1:n.303+73A=
NM_030662.4:c.303+73A= MANE Select NP_109587.1:n.303+73A=