Canonical Allele Identifier: CA2584876566

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4090498-AGGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090505_4090508del , CM000681.2:g.4090505_4090508del	GRCh38
NC_000019.9:g.4090503_4090506del , CM000681.1:g.4090503_4090506del	GRCh37
NC_000019.8:g.4041503_4041506del	NCBI36
NG_007996.1:g.38627_38630del , LRG_750:g.38627_38630del

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1738_1741del
ENST00000688002.1:n.3450_3453del
ENST00000688751.1:n.435_438del
ENST00000689792.1:n.1203_1206del
ENST00000262948.10:c.*96_*99del MANE Select	ENSP00000262948.4:n.*96_*99del
ENST00000262948.9:c.*96_*99del	ENSP00000262948.3:n.*96_*99del
ENST00000394867.8:c.*96_*99del	ENSP00000378336.1:n.*96_*99del
ENST00000597263.5:n.484_487del
ENST00000600584.5:n.2748_2751del
ENST00000601786.5:n.1600_1603del
NM_030662.3:c.*96_*99del , LRG_750t1:c.*96_*99del	NP_109587.1:n.*96_*99del
XM_006722799.2:c.*96_*99del	XP_006722862.1:n.*96_*99del
XM_011528133.1:c.*96_*99del	XP_011526435.1:n.*96_*99del
NM_030662.4:c.*96_*99del MANE Select	NP_109587.1:n.*96_*99del