Canonical Allele Identifier: CA403381142
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090690G>C , CM000681.2:g.4090690G>C GRCh38
NC_000019.9:g.4090688G>C , CM000681.1:g.4090688G>C GRCh37
NC_000019.8:g.4041688G>C NCBI36
NG_007996.1:g.38439C>G , LRG_750:g.38439C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1550C>G
ENST00000688002.1:n.3262C>G
ENST00000688751.1:n.247C>G
ENST00000689792.1:n.1015C>G
ENST00000262948.10:c.1111C>G MANE Select ENSP00000262948.4:p.Arg371Gly
ENST00000262948.9:c.1111C>G ENSP00000262948.3:p.Arg371Gly
ENST00000394867.8:c.820C>G ENSP00000378336.1:p.Arg274Gly
ENST00000597263.5:n.296C>G
ENST00000599021.1:c.221C>G
ENST00000600584.5:n.2560C>G
ENST00000601786.5:n.1412C>G
NM_030662.3:c.1111C>G , LRG_750t1:c.1111C>G NP_109587.1:p.Arg371Gly
XM_006722799.2:c.832C>G XP_006722862.1:p.Arg278Gly
XM_011528133.1:c.541C>G XP_011526435.1:p.Arg181Gly
NM_030662.4:c.1111C>G MANE Select NP_109587.1:p.Arg371Gly