Canonical Allele Identifier: CA2584876508

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4090438-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090443del , CM000681.2:g.4090443del	GRCh38
NC_000019.9:g.4090441del , CM000681.1:g.4090441del	GRCh37
NC_000019.8:g.4041441del	NCBI36
NG_007996.1:g.38690del , LRG_750:g.38690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1801del
ENST00000688751.1:n.498del
ENST00000689792.1:n.1266del
ENST00000262948.10:c.*159del MANE Select	ENSP00000262948.4:n.*159del
ENST00000262948.9:c.*159del	ENSP00000262948.3:n.*159del
ENST00000394867.8:c.*159del	ENSP00000378336.1:n.*159del
ENST00000597263.5:n.547del
ENST00000600584.5:n.2811del
ENST00000601786.5:n.1663del
NM_030662.3:c.*159del , LRG_750t1:c.*159del	NP_109587.1:n.*159del
XM_006722799.2:c.*159del	XP_006722862.1:n.*159del
XM_011528133.1:c.*159del	XP_011526435.1:n.*159del
NM_030662.4:c.*159del MANE Select	NP_109587.1:n.*159del