Canonical Allele Identifier: CA2584877127

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094666-GGAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094669_4094671del , CM000681.2:g.4094669_4094671del	GRCh38
NC_000019.9:g.4094667_4094669del , CM000681.1:g.4094667_4094669del	GRCh37
NC_000019.8:g.4045667_4045669del	NCBI36
NG_007996.1:g.34460_34462del , LRG_750:g.34460_34462del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-171_1486-169del
ENST00000688002.1:n.3198-171_3198-169del
ENST00000688751.1:n.183-171_183-169del
ENST00000689792.1:n.951-171_951-169del
ENST00000262948.10:c.1047-171_1047-169del MANE Select	ENSP00000262948.4:n.1047-171_1047-169del
ENST00000262948.9:c.1047-171_1047-169del	ENSP00000262948.3:n.1047-171_1047-169del
ENST00000394867.8:c.756-171_756-169del	ENSP00000378336.1:n.756-171_756-169del
ENST00000597263.5:n.232-171_232-169del
ENST00000599021.1:c.157-171_157-169del
ENST00000600584.5:n.2325_2327del
ENST00000601786.5:n.1348-171_1348-169del
NM_030662.3:c.1047-171_1047-169del , LRG_750t1:c.1047-171_1047-169del	NP_109587.1:n.1047-171_1047-169del
XM_006722799.2:c.768-171_768-169del	XP_006722862.1:n.768-171_768-169del
XM_011528133.1:c.477-171_477-169del	XP_011526435.1:n.477-171_477-169del
XM_017026989.1:c.1424_1426del	XP_016882478.1:p.Arg475del
XM_017026990.1:c.1145_1147del	XP_016882479.1:p.Arg382del
NM_030662.4:c.1047-171_1047-169del MANE Select	NP_109587.1:n.1047-171_1047-169del