Canonical Allele Identifier: CA2319222363
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4095625_4095627delinsTGA , CM000681.2:g.4095625_4095627delinsTGA GRCh38
NC_000019.9:g.4095623_4095625delinsTGA , CM000681.1:g.4095623_4095625delinsTGA GRCh37
NC_000019.8:g.4046623_4046625delinsTGA NCBI36
NG_007996.1:g.33502_33504delinsTCA , LRG_750:g.33502_33504delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1424-178_1424-176delinsTCA
ENST00000688002.1:n.3136-178_3136-176delinsTCA
ENST00000688751.1:n.121-178_121-176delinsTCA
ENST00000689792.1:n.889-178_889-176delinsTCA
ENST00000262948.10:c.985-178_985-176delinsTCA MANE Select ENSP00000262948.4:n.985-178_985-176delinsTCA
ENST00000262948.9:c.985-178_985-176delinsTCA ENSP00000262948.3:n.985-178_985-176delinsTCA
ENST00000394867.8:c.694-178_694-176delinsTCA ENSP00000378336.1:n.694-178_694-176delinsTCA
ENST00000595715.1:n.800-178_800-176delinsTCA
ENST00000597263.5:n.170-178_170-176delinsTCA
ENST00000599021.1:c.95-178_95-176delinsTCA
ENST00000600584.5:n.1545-178_1545-176delinsTCA
ENST00000601786.5:n.1286-178_1286-176delinsTCA
NM_030662.3:c.985-178_985-176delinsTCA , LRG_750t1:c.985-178_985-176delinsTCA NP_109587.1:n.985-178_985-176delinsTCA
XM_006722799.2:c.706-178_706-176delinsTCA XP_006722862.1:n.706-178_706-176delinsTCA
XM_011528133.1:c.415-178_415-176delinsTCA XP_011526435.1:n.415-178_415-176delinsTCA
XM_017026989.1:c.985-178_985-176delinsTCA XP_016882478.1:n.985-178_985-176delinsTCA
XM_017026990.1:c.706-178_706-176delinsTCA XP_016882479.1:n.706-178_706-176delinsTCA
NM_030662.4:c.985-178_985-176delinsTCA MANE Select NP_109587.1:n.985-178_985-176delinsTCA