Canonical Allele Identifier: CA2813356130
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090816_4090817insACCCCAAACACACCCAACA , CM000681.2:g.4090816_4090817insACCCCAAACACACCCAACA GRCh38
NC_000019.9:g.4090814_4090815insACCCCAAACACACCCAACA , CM000681.1:g.4090814_4090815insACCCCAAACACACCCAACA GRCh37
NC_000019.8:g.4041814_4041815insACCCCAAACACACCCAACA NCBI36
NG_007996.1:g.38313_38314insGTTGGGTGTGTTTGGGGTT , LRG_750:g.38313_38314insGTTGGGTGTGTTTGGGGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1532-108_1532-107insGTTGGGTGTGTTTGGGGTT
ENST00000688002.1:n.3244-108_3244-107insGTTGGGTGTGTTTGGGGTT
ENST00000688751.1:n.229-108_229-107insGTTGGGTGTGTTTGGGGTT
ENST00000689792.1:n.997-108_997-107insGTTGGGTGTGTTTGGGGTT
ENST00000262948.10:c.1093-108_1093-107insGTTGGGTGTGTTTGGGGTT MANE Select ENSP00000262948.4:n.1093-108_1093-107insGTTGGGTGTGTTTGGGGTT
ENST00000262948.9:c.1093-108_1093-107insGTTGGGTGTGTTTGGGGTT ENSP00000262948.3:n.1093-108_1093-107insGTTGGGTGTGTTTGGGGTT
ENST00000394867.8:c.802-108_802-107insGTTGGGTGTGTTTGGGGTT ENSP00000378336.1:n.802-108_802-107insGTTGGGTGTGTTTGGGGTT
ENST00000597263.5:n.278-108_278-107insGTTGGGTGTGTTTGGGGTT
ENST00000599021.1:c.203-108_203-107insGTTGGGTGTGTTTGGGGTT
ENST00000600584.5:n.2542-108_2542-107insGTTGGGTGTGTTTGGGGTT
ENST00000601786.5:n.1394-108_1394-107insGTTGGGTGTGTTTGGGGTT
NM_030662.3:c.1093-108_1093-107insGTTGGGTGTGTTTGGGGTT , LRG_750t1:c.1093-108_1093-107insGTTGGGTGTGTTTGGGGTT NP_109587.1:n.1093-108_1093-107insGTTGGGTGTGTTTGGGGTT
XM_006722799.2:c.814-108_814-107insGTTGGGTGTGTTTGGGGTT XP_006722862.1:n.814-108_814-107insGTTGGGTGTGTTTGGGGTT
XM_011528133.1:c.523-108_523-107insGTTGGGTGTGTTTGGGGTT XP_011526435.1:n.523-108_523-107insGTTGGGTGTGTTTGGGGTT
NM_030662.4:c.1093-108_1093-107insGTTGGGTGTGTTTGGGGTT MANE Select NP_109587.1:n.1093-108_1093-107insGTTGGGTGTGTTTGGGGTT