Canonical Allele Identifier: CA2584876565

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4090498-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090501dup , CM000681.2:g.4090501dup	GRCh38
NC_000019.9:g.4090499dup , CM000681.1:g.4090499dup	GRCh37
NC_000019.8:g.4041499dup	NCBI36
NG_007996.1:g.38630dup , LRG_750:g.38630dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1741dup
ENST00000688002.1:n.3453dup
ENST00000688751.1:n.438dup
ENST00000689792.1:n.1206dup
ENST00000262948.10:c.*99dup MANE Select	ENSP00000262948.4:n.*99dup
ENST00000262948.9:c.*99dup	ENSP00000262948.3:n.*99dup
ENST00000394867.8:c.*99dup	ENSP00000378336.1:n.*99dup
ENST00000597263.5:n.487dup
ENST00000600584.5:n.2751dup
ENST00000601786.5:n.1603dup
NM_030662.3:c.*99dup , LRG_750t1:c.*99dup	NP_109587.1:n.*99dup
XM_006722799.2:c.*99dup	XP_006722862.1:n.*99dup
XM_011528133.1:c.*99dup	XP_011526435.1:n.*99dup
NM_030662.4:c.*99dup MANE Select	NP_109587.1:n.*99dup