Canonical Allele Identifier: CA2584876505

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4090438-A-AC

Genomic Alleles

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

Transcript Alleles

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