Canonical Allele Identifier: CA2319222350

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095594_4095596delinsCAG , CM000681.2:g.4095594_4095596delinsCAG	GRCh38
NC_000019.9:g.4095592_4095594delinsCAG , CM000681.1:g.4095592_4095594delinsCAG	GRCh37
NC_000019.8:g.4046592_4046594delinsCAG	NCBI36
NG_007996.1:g.33533_33535delinsCTG , LRG_750:g.33533_33535delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-147_1424-145delinsCTG
ENST00000688002.1:n.3136-147_3136-145delinsCTG
ENST00000688751.1:n.121-147_121-145delinsCTG
ENST00000689792.1:n.889-147_889-145delinsCTG
ENST00000262948.10:c.985-147_985-145delinsCTG MANE Select	ENSP00000262948.4:n.985-147_985-145delinsCTG
ENST00000262948.9:c.985-147_985-145delinsCTG	ENSP00000262948.3:n.985-147_985-145delinsCTG
ENST00000394867.8:c.694-147_694-145delinsCTG	ENSP00000378336.1:n.694-147_694-145delinsCTG
ENST00000595715.1:n.800-147_800-145delinsCTG
ENST00000597263.5:n.170-147_170-145delinsCTG
ENST00000599021.1:c.95-147_95-145delinsCTG
ENST00000600584.5:n.1545-147_1545-145delinsCTG
ENST00000601786.5:n.1286-147_1286-145delinsCTG
NM_030662.3:c.985-147_985-145delinsCTG , LRG_750t1:c.985-147_985-145delinsCTG	NP_109587.1:n.985-147_985-145delinsCTG
XM_006722799.2:c.706-147_706-145delinsCTG	XP_006722862.1:n.706-147_706-145delinsCTG
XM_011528133.1:c.415-147_415-145delinsCTG	XP_011526435.1:n.415-147_415-145delinsCTG
XM_017026989.1:c.985-147_985-145delinsCTG	XP_016882478.1:n.985-147_985-145delinsCTG
XM_017026990.1:c.706-147_706-145delinsCTG	XP_016882479.1:n.706-147_706-145delinsCTG
NM_030662.4:c.985-147_985-145delinsCTG MANE Select	NP_109587.1:n.985-147_985-145delinsCTG