Canonical Allele Identifier: CA2319224356

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099212_4099221delinsCGCCCGGGGG , CM000681.2:g.4099212_4099221delinsCGCCCGGGGG	GRCh38
NC_000019.9:g.4099210_4099219delinsCGCCCGGGGG , CM000681.1:g.4099210_4099219delinsCGCCCGGGGG	GRCh37
NC_000019.8:g.4050210_4050219delinsCGCCCGGGGG	NCBI36
NG_007996.1:g.29908_29917delinsCCCCCGGGCG , LRG_750:g.29908_29917delinsCCCCCGGGCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1338_1347delinsCCCCCGGGCG
ENST00000687128.1:n.1338_1347delinsCCCCCGGGCG
ENST00000688002.1:n.1193_1202delinsCCCCCGGGCG
ENST00000689792.1:n.803_812delinsCCCCCGGGCG
ENST00000262948.10:c.899_908delinsCCCCCGGGCG MANE Select	ENSP00000262948.4:p.Pro300=
ENST00000262948.9:c.899_908delinsCCCCCGGGCG	ENSP00000262948.3:p.Pro300=
ENST00000394867.8:c.608_617delinsCCCCCGGGCG	ENSP00000378336.1:p.Pro203=
ENST00000593364.5:n.846_855delinsCCCCCGGGCG
ENST00000595715.1:n.714_723delinsCCCCCGGGCG
ENST00000597263.5:n.169+1798_169+1807delinsCCCCCGGGCG
ENST00000599021.1:c.29+1798_29+1807delinsCCCCCGGGCG
ENST00000600584.5:n.1459_1468delinsCCCCCGGGCG
ENST00000601786.5:n.1200_1209delinsCCCCCGGGCG
NM_030662.3:c.899_908delinsCCCCCGGGCG , LRG_750t1:c.899_908delinsCCCCCGGGCG	NP_109587.1:p.Pro300=
XM_006722799.2:c.705+1798_705+1807delinsCCCCCGGGCG	XP_006722862.1:n.705+1798_705+1807delinsC...
XM_011528133.1:c.329_338delinsCCCCCGGGCG	XP_011526435.1:p.Pro110=
XM_017026989.1:c.899_908delinsCCCCCGGGCG	XP_016882478.1:p.Pro300=
XM_017026990.1:c.705+1798_705+1807delinsCCCCCGGGCG	XP_016882479.1:n.705+1798_705+1807delinsC...
NM_030662.4:c.899_908delinsCCCCCGGGCG MANE Select	NP_109587.1:p.Pro300=