Canonical Allele Identifier: CA2584876630

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4090550-AGGGACGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090554_4090561del , CM000681.2:g.4090554_4090561del	GRCh38
NC_000019.9:g.4090552_4090559del , CM000681.1:g.4090552_4090559del	GRCh37
NC_000019.8:g.4041552_4041559del	NCBI36
NG_007996.1:g.38571_38578del , LRG_750:g.38571_38578del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1682_1689del
ENST00000688002.1:n.3394_3401del
ENST00000688751.1:n.379_386del
ENST00000689792.1:n.1147_1154del
ENST00000262948.10:c.*40_*47del MANE Select	ENSP00000262948.4:n.*40_*47del
ENST00000262948.9:c.*40_*47del	ENSP00000262948.3:n.*40_*47del
ENST00000394867.8:c.*40_*47del	ENSP00000378336.1:n.*40_*47del
ENST00000597263.5:n.428_435del
ENST00000600584.5:n.2692_2699del
ENST00000601786.5:n.1544_1551del
NM_030662.3:c.*40_*47del , LRG_750t1:c.*40_*47del	NP_109587.1:n.*40_*47del
XM_006722799.2:c.*40_*47del	XP_006722862.1:n.*40_*47del
XM_011528133.1:c.*40_*47del	XP_011526435.1:n.*40_*47del
NM_030662.4:c.*40_*47del MANE Select	NP_109587.1:n.*40_*47del