Canonical Allele Identifier: CA2319224299

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099119_4099120delinsGA , CM000681.2:g.4099119_4099120delinsGA	GRCh38
NC_000019.9:g.4099117_4099118delinsGA , CM000681.1:g.4099117_4099118delinsGA	GRCh37
NC_000019.8:g.4050117_4050118delinsGA	NCBI36
NG_007996.1:g.30009_30010delinsTC , LRG_750:g.30009_30010delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1358+81_1358+82delinsTC
ENST00000687128.1:n.1439_1440delinsTC
ENST00000688002.1:n.1294_1295delinsTC
ENST00000689792.1:n.823+81_823+82delinsTC
ENST00000262948.10:c.919+81_919+82delinsTC MANE Select	ENSP00000262948.4:n.919+81_919+82delinsTC
ENST00000262948.9:c.919+81_919+82delinsTC	ENSP00000262948.3:n.919+81_919+82delinsTC
ENST00000394867.8:c.628+81_628+82delinsTC	ENSP00000378336.1:n.628+81_628+82delinsTC
ENST00000595715.1:n.734+81_734+82delinsTC
ENST00000597263.5:n.169+1899_169+1900delinsTC
ENST00000599021.1:c.30-1777_30-1776delinsTC
ENST00000600584.5:n.1479+81_1479+82delinsTC
ENST00000601786.5:n.1220+81_1220+82delinsTC
NM_030662.3:c.919+81_919+82delinsTC , LRG_750t1:c.919+81_919+82delinsTC	NP_109587.1:n.919+81_919+82delinsTC
XM_006722799.2:c.705+1899_705+1900delinsTC	XP_006722862.1:n.705+1899_705+1900delinsTC
XM_011528133.1:c.349+81_349+82delinsTC	XP_011526435.1:n.349+81_349+82delinsTC
XM_017026989.1:c.919+81_919+82delinsTC	XP_016882478.1:n.919+81_919+82delinsTC
XM_017026990.1:c.705+1899_705+1900delinsTC	XP_016882479.1:n.705+1899_705+1900delinsTC
NM_030662.4:c.919+81_919+82delinsTC MANE Select	NP_109587.1:n.919+81_919+82delinsTC