Canonical Allele Identifier: CA2584877159

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094706-GACACCCCCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094708_4094716del , CM000681.2:g.4094708_4094716del	GRCh38
NC_000019.9:g.4094706_4094714del , CM000681.1:g.4094706_4094714del	GRCh37
NC_000019.8:g.4045706_4045714del	NCBI36
NG_007996.1:g.34414_34422del , LRG_750:g.34414_34422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-217_1486-209del
ENST00000688002.1:n.3198-217_3198-209del
ENST00000688751.1:n.183-217_183-209del
ENST00000689792.1:n.951-217_951-209del
ENST00000262948.10:c.1047-217_1047-209del MANE Select	ENSP00000262948.4:n.1047-217_1047-209del
ENST00000262948.9:c.1047-217_1047-209del	ENSP00000262948.3:n.1047-217_1047-209del
ENST00000394867.8:c.756-217_756-209del	ENSP00000378336.1:n.756-217_756-209del
ENST00000597263.5:n.232-217_232-209del
ENST00000599021.1:c.157-217_157-209del
ENST00000600584.5:n.2279_2287del
ENST00000601786.5:n.1348-217_1348-209del
NM_030662.3:c.1047-217_1047-209del , LRG_750t1:c.1047-217_1047-209del	NP_109587.1:n.1047-217_1047-209del
XM_006722799.2:c.768-217_768-209del	XP_006722862.1:n.768-217_768-209del
XM_011528133.1:c.477-217_477-209del	XP_011526435.1:n.477-217_477-209del
XM_017026989.1:c.1378_1386del	XP_016882478.1:p.Gly460_Cys462del
XM_017026990.1:c.1099_1107del	XP_016882479.1:p.Gly367_Cys369del
NM_030662.4:c.1047-217_1047-209del MANE Select	NP_109587.1:n.1047-217_1047-209del