Canonical Allele Identifier: CA2319224271

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099076_4099077delinsCG , CM000681.2:g.4099076_4099077delinsCG	GRCh38
NC_000019.9:g.4099074_4099075delinsCG , CM000681.1:g.4099074_4099075delinsCG	GRCh37
NC_000019.8:g.4050074_4050075delinsCG	NCBI36
NG_007996.1:g.30052_30053delinsCG , LRG_750:g.30052_30053delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+124_1358+125delinsCG
ENST00000687128.1:n.1482_1483delinsCG
ENST00000688002.1:n.1337_1338delinsCG
ENST00000689792.1:n.823+124_823+125delinsCG
ENST00000262948.10:c.919+124_919+125delinsCG MANE Select	ENSP00000262948.4:n.919+124_919+125delinsCG
ENST00000262948.9:c.919+124_919+125delinsCG	ENSP00000262948.3:n.919+124_919+125delinsCG
ENST00000394867.8:c.628+124_628+125delinsCG	ENSP00000378336.1:n.628+124_628+125delinsCG
ENST00000595715.1:n.734+124_734+125delinsCG
ENST00000597263.5:n.169+1942_169+1943delinsCG
ENST00000599021.1:c.30-1734_30-1733delinsCG
ENST00000600584.5:n.1479+124_1479+125delinsCG
ENST00000601786.5:n.1220+124_1220+125delinsCG
NM_030662.3:c.919+124_919+125delinsCG , LRG_750t1:c.919+124_919+125delinsCG	NP_109587.1:n.919+124_919+125delinsCG
XM_006722799.2:c.705+1942_705+1943delinsCG	XP_006722862.1:n.705+1942_705+1943delinsCG
XM_011528133.1:c.349+124_349+125delinsCG	XP_011526435.1:n.349+124_349+125delinsCG
XM_017026989.1:c.919+124_919+125delinsCG	XP_016882478.1:n.919+124_919+125delinsCG
XM_017026990.1:c.705+1942_705+1943delinsCG	XP_016882479.1:n.705+1942_705+1943delinsCG
NM_030662.4:c.919+124_919+125delinsCG MANE Select	NP_109587.1:n.919+124_919+125delinsCG