Canonical Allele Identifier: CA2319234283

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117434_4117435delinsGA , CM000681.2:g.4117434_4117435delinsGA	GRCh38
NC_000019.9:g.4117432_4117433delinsGA , CM000681.1:g.4117432_4117433delinsGA	GRCh37
NC_000019.8:g.4068432_4068433delinsGA	NCBI36
NG_007996.1:g.11694_11695delinsTC , LRG_750:g.11694_11695delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.726_727delinsTC
ENST00000687128.1:n.726_727delinsTC
ENST00000262948.10:c.287_288delinsTC MANE Select	ENSP00000262948.4:p.Leu96=
ENST00000262948.9:c.287_288delinsTC	ENSP00000262948.3:p.Leu96=
ENST00000394867.8:c.-5_-4delinsTC	ENSP00000378336.1:n.-5_-4delinsTC
ENST00000599345.1:n.484_485delinsTC
NM_030662.3:c.287_288delinsTC , LRG_750t1:c.287_288delinsTC	NP_109587.1:p.Leu96=
XM_006722799.2:c.287_288delinsTC	XP_006722862.1:p.Leu96=
XM_017026989.1:c.287_288delinsTC	XP_016882478.1:p.Leu96=
XM_017026990.1:c.287_288delinsTC	XP_016882479.1:p.Leu96=
XM_017026991.1:c.287_288delinsTC	XP_016882480.1:p.Leu96=
NM_030662.4:c.287_288delinsTC MANE Select	NP_109587.1:p.Leu96=