Canonical Allele Identifier: CA2584877895

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4095480-CCTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095481_4095483del , CM000681.2:g.4095481_4095483del	GRCh38
NC_000019.9:g.4095479_4095481del , CM000681.1:g.4095479_4095481del	GRCh37
NC_000019.8:g.4046479_4046481del	NCBI36
NG_007996.1:g.33646_33648del , LRG_750:g.33646_33648del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-34_1424-32del
ENST00000688002.1:n.3136-34_3136-32del
ENST00000688751.1:n.121-34_121-32del
ENST00000689792.1:n.889-34_889-32del
ENST00000262948.10:c.985-34_985-32del MANE Select	ENSP00000262948.4:n.985-34_985-32del
ENST00000262948.9:c.985-34_985-32del	ENSP00000262948.3:n.985-34_985-32del
ENST00000394867.8:c.694-34_694-32del	ENSP00000378336.1:n.694-34_694-32del
ENST00000595715.1:n.800-34_800-32del
ENST00000597263.5:n.170-34_170-32del
ENST00000599021.1:c.95-34_95-32del
ENST00000600584.5:n.1545-34_1545-32del
ENST00000601786.5:n.1286-34_1286-32del
NM_030662.3:c.985-34_985-32del , LRG_750t1:c.985-34_985-32del	NP_109587.1:n.985-34_985-32del
XM_006722799.2:c.706-34_706-32del	XP_006722862.1:n.706-34_706-32del
XM_011528133.1:c.415-34_415-32del	XP_011526435.1:n.415-34_415-32del
XM_017026989.1:c.985-34_985-32del	XP_016882478.1:n.985-34_985-32del
XM_017026990.1:c.706-34_706-32del	XP_016882479.1:n.706-34_706-32del
NM_030662.4:c.985-34_985-32del MANE Select	NP_109587.1:n.985-34_985-32del