Canonical Allele Identifier: CA2319219684
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090522_4090523delinsTC , CM000681.2:g.4090522_4090523delinsTC GRCh38
NC_000019.9:g.4090520_4090521delinsTC , CM000681.1:g.4090520_4090521delinsTC GRCh37
NC_000019.8:g.4041520_4041521delinsTC NCBI36
NG_007996.1:g.38606_38607delinsGA , LRG_750:g.38606_38607delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1717_1718delinsGA
ENST00000688002.1:n.3429_3430delinsGA
ENST00000688751.1:n.414_415delinsGA
ENST00000689792.1:n.1182_1183delinsGA
ENST00000262948.10:c.*75_*76delinsGA MANE Select ENSP00000262948.4:n.*75_*76delinsGA
ENST00000262948.9:c.*75_*76delinsGA ENSP00000262948.3:n.*75_*76delinsGA
ENST00000394867.8:c.*75_*76delinsGA ENSP00000378336.1:n.*75_*76delinsGA
ENST00000597263.5:n.463_464delinsGA
ENST00000600584.5:n.2727_2728delinsGA
ENST00000601786.5:n.1579_1580delinsGA
NM_030662.3:c.*75_*76delinsGA , LRG_750t1:c.*75_*76delinsGA NP_109587.1:n.*75_*76delinsGA
XM_006722799.2:c.*75_*76delinsGA XP_006722862.1:n.*75_*76delinsGA
XM_011528133.1:c.*75_*76delinsGA XP_011526435.1:n.*75_*76delinsGA
NM_030662.4:c.*75_*76delinsGA MANE Select NP_109587.1:n.*75_*76delinsGA