Canonical Allele Identifier: CA2584877125

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094664-G-GAAC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094665_4094666insACA , CM000681.2:g.4094665_4094666insACA	GRCh38
NC_000019.9:g.4094663_4094664insACA , CM000681.1:g.4094663_4094664insACA	GRCh37
NC_000019.8:g.4045663_4045664insACA	NCBI36
NG_007996.1:g.34464_34465insGTT , LRG_750:g.34464_34465insGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-167_1486-166insGTT
ENST00000688002.1:n.3198-167_3198-166insGTT
ENST00000688751.1:n.183-167_183-166insGTT
ENST00000689792.1:n.951-167_951-166insGTT
ENST00000262948.10:c.1047-167_1047-166insGTT MANE Select	ENSP00000262948.4:n.1047-167_1047-166insGTT
ENST00000262948.9:c.1047-167_1047-166insGTT	ENSP00000262948.3:n.1047-167_1047-166insGTT
ENST00000394867.8:c.756-167_756-166insGTT	ENSP00000378336.1:n.756-167_756-166insGTT
ENST00000597263.5:n.232-167_232-166insGTT
ENST00000599021.1:c.157-167_157-166insGTT
ENST00000600584.5:n.2329_2330insGTT
ENST00000601786.5:n.1348-167_1348-166insGTT
NM_030662.3:c.1047-167_1047-166insGTT , LRG_750t1:c.1047-167_1047-166insGTT	NP_109587.1:n.1047-167_1047-166insGTT
XM_006722799.2:c.768-167_768-166insGTT	XP_006722862.1:n.768-167_768-166insGTT
XM_011528133.1:c.477-167_477-166insGTT	XP_011526435.1:n.477-167_477-166insGTT
XM_017026989.1:c.1428_1429insGTT	XP_016882478.1:p.Pro476_Leu477insVal
XM_017026990.1:c.1149_1150insGTT	XP_016882479.1:p.Pro383_Leu384insVal
NM_030662.4:c.1047-167_1047-166insGTT MANE Select	NP_109587.1:n.1047-167_1047-166insGTT