Canonical Allele Identifier: CA2584878621
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4099547_4099548insAGATCGGAAGA , CM000681.2:g.4099547_4099548insAGATCGGAAGA GRCh38
NC_000019.9:g.4099545_4099546insAGATCGGAAGA , CM000681.1:g.4099545_4099546insAGATCGGAAGA GRCh37
NC_000019.8:g.4050545_4050546insAGATCGGAAGA NCBI36
NG_007996.1:g.29581_29582insTCTTCCGATCT , LRG_750:g.29581_29582insTCTTCCGATCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1145-134_1145-133insTCTTCCGATCT
ENST00000687128.1:n.1145-134_1145-133insTCTTCCGATCT
ENST00000688002.1:n.866_867insTCTTCCGATCT
ENST00000689792.1:n.646-170_646-169insTCTTCCGATCT
ENST00000262948.10:c.706-134_706-133insTCTTCCGATCT MANE Select ENSP00000262948.4:n.706-134_706-133insTCTTCCGATCT
ENST00000262948.9:c.706-134_706-133insTCTTCCGATCT ENSP00000262948.3:n.706-134_706-133insTCTTCCGATCT
ENST00000394867.8:c.415-134_415-133insTCTTCCGATCT ENSP00000378336.1:n.415-134_415-133insTCTTCCGATCT
ENST00000593364.5:n.653-134_653-133insTCTTCCGATCT
ENST00000595715.1:n.387_388insTCTTCCGATCT
ENST00000597263.5:n.169+1471_169+1472insTCTTCCGATCT
ENST00000599021.1:c.29+1471_29+1472insTCTTCCGATCT
ENST00000600584.5:n.1132_1133insTCTTCCGATCT
ENST00000601786.5:n.1007-134_1007-133insTCTTCCGATCT
ENST00000602167.5:n.426-134_426-133insTCTTCCGATCT
NM_030662.3:c.706-134_706-133insTCTTCCGATCT , LRG_750t1:c.706-134_706-133insTCTTCCGATCT NP_109587.1:n.706-134_706-133insTCTTCCGATCT
XM_006722799.2:c.705+1471_705+1472insTCTTCCGATCT XP_006722862.1:n.705+1471_705+1472insTCTTCCGATCT
XM_011528133.1:c.136-134_136-133insTCTTCCGATCT XP_011526435.1:n.136-134_136-133insTCTTCCGATCT
XM_017026989.1:c.706-134_706-133insTCTTCCGATCT XP_016882478.1:n.706-134_706-133insTCTTCCGATCT
XM_017026990.1:c.705+1471_705+1472insTCTTCCGATCT XP_016882479.1:n.705+1471_705+1472insTCTTCCGATCT
XM_017026991.1:c.*182_*183insTCTTCCGATCT XP_016882480.1:n.*182_*183insTCTTCCGATCT
NM_030662.4:c.706-134_706-133insTCTTCCGATCT MANE Select NP_109587.1:n.706-134_706-133insTCTTCCGATCT