Canonical Allele Identifier: CA2576573099

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4090506-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090508del , CM000681.2:g.4090508del	GRCh38
NC_000019.9:g.4090506del , CM000681.1:g.4090506del	GRCh37
NC_000019.8:g.4041506del	NCBI36
NG_007996.1:g.38622del , LRG_750:g.38622del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1733del
ENST00000688002.1:n.3445del
ENST00000688751.1:n.430del
ENST00000689792.1:n.1198del
ENST00000262948.10:c.*91del MANE Select	ENSP00000262948.4:n.*91del
ENST00000262948.9:c.*91del	ENSP00000262948.3:n.*91del
ENST00000394867.8:c.*91del	ENSP00000378336.1:n.*91del
ENST00000597263.5:n.479del
ENST00000600584.5:n.2743del
ENST00000601786.5:n.1595del
NM_030662.3:c.*91del , LRG_750t1:c.*91del	NP_109587.1:n.*91del
XM_006722799.2:c.*91del	XP_006722862.1:n.*91del
XM_011528133.1:c.*91del	XP_011526435.1:n.*91del
NM_030662.4:c.*91del MANE Select	NP_109587.1:n.*91del