Canonical Allele Identifier: CA2319219728

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090589_4090590delinsCG , CM000681.2:g.4090589_4090590delinsCG	GRCh38
NC_000019.9:g.4090587_4090588delinsCG , CM000681.1:g.4090587_4090588delinsCG	GRCh37
NC_000019.8:g.4041587_4041588delinsCG	NCBI36
NG_007996.1:g.38539_38540delinsCG , LRG_750:g.38539_38540delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1650_1651delinsCG
ENST00000688002.1:n.3362_3363delinsCG
ENST00000688751.1:n.347_348delinsCG
ENST00000689792.1:n.1115_1116delinsCG
ENST00000262948.10:c.*8_*9delinsCG MANE Select	ENSP00000262948.4:n.*8_*9delinsCG
ENST00000262948.9:c.*8_*9delinsCG	ENSP00000262948.3:n.*8_*9delinsCG
ENST00000394867.8:c.*8_*9delinsCG	ENSP00000378336.1:n.*8_*9delinsCG
ENST00000597263.5:n.396_397delinsCG
ENST00000600584.5:n.2660_2661delinsCG
ENST00000601786.5:n.1512_1513delinsCG
NM_030662.3:c.*8_*9delinsCG , LRG_750t1:c.*8_*9delinsCG	NP_109587.1:n.*8_*9delinsCG
XM_006722799.2:c.*8_*9delinsCG	XP_006722862.1:n.*8_*9delinsCG
XM_011528133.1:c.*8_*9delinsCG	XP_011526435.1:n.*8_*9delinsCG
NM_030662.4:c.*8_*9delinsCG MANE Select	NP_109587.1:n.*8_*9delinsCG