Canonical Allele Identifier: CA2319222344

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095589_4095591delinsCCT , CM000681.2:g.4095589_4095591delinsCCT	GRCh38
NC_000019.9:g.4095587_4095589delinsCCT , CM000681.1:g.4095587_4095589delinsCCT	GRCh37
NC_000019.8:g.4046587_4046589delinsCCT	NCBI36
NG_007996.1:g.33538_33540delinsAGG , LRG_750:g.33538_33540delinsAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1424-142_1424-140delinsAGG
ENST00000688002.1:n.3136-142_3136-140delinsAGG
ENST00000688751.1:n.121-142_121-140delinsAGG
ENST00000689792.1:n.889-142_889-140delinsAGG
ENST00000262948.10:c.985-142_985-140delinsAGG MANE Select	ENSP00000262948.4:n.985-142_985-140delinsAGG
ENST00000262948.9:c.985-142_985-140delinsAGG	ENSP00000262948.3:n.985-142_985-140delinsAGG
ENST00000394867.8:c.694-142_694-140delinsAGG	ENSP00000378336.1:n.694-142_694-140delinsAGG
ENST00000595715.1:n.800-142_800-140delinsAGG
ENST00000597263.5:n.170-142_170-140delinsAGG
ENST00000599021.1:c.95-142_95-140delinsAGG
ENST00000600584.5:n.1545-142_1545-140delinsAGG
ENST00000601786.5:n.1286-142_1286-140delinsAGG
NM_030662.3:c.985-142_985-140delinsAGG , LRG_750t1:c.985-142_985-140delinsAGG	NP_109587.1:n.985-142_985-140delinsAGG
XM_006722799.2:c.706-142_706-140delinsAGG	XP_006722862.1:n.706-142_706-140delinsAGG
XM_011528133.1:c.415-142_415-140delinsAGG	XP_011526435.1:n.415-142_415-140delinsAGG
XM_017026989.1:c.985-142_985-140delinsAGG	XP_016882478.1:n.985-142_985-140delinsAGG
XM_017026990.1:c.706-142_706-140delinsAGG	XP_016882479.1:n.706-142_706-140delinsAGG
NM_030662.4:c.985-142_985-140delinsAGG MANE Select	NP_109587.1:n.985-142_985-140delinsAGG