Canonical Allele Identifier: CA2576573095
Gene: MAP2K2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090491_4090503del , CM000681.2:g.4090491_4090503del GRCh38
NC_000019.9:g.4090489_4090501del , CM000681.1:g.4090489_4090501del GRCh37
NC_000019.8:g.4041489_4041501del NCBI36
NG_007996.1:g.38631_38643del , LRG_750:g.38631_38643del

Transcript Alleles

HGVS Amino-acid change
ENST00000394867.9:n.1742_1754del
ENST00000688002.1:n.3454_3466del
ENST00000688751.1:n.439_451del
ENST00000689792.1:n.1207_1219del
ENST00000262948.10:c.*100_*112del MANE Select ENSP00000262948.4:n.*100_*112del
ENST00000262948.9:c.*100_*112del ENSP00000262948.3:n.*100_*112del
ENST00000394867.8:c.*100_*112del ENSP00000378336.1:n.*100_*112del
ENST00000597263.5:n.488_500del
ENST00000600584.5:n.2752_2764del
ENST00000601786.5:n.1604_1616del
NM_030662.3:c.*100_*112del , LRG_750t1:c.*100_*112del NP_109587.1:n.*100_*112del
XM_006722799.2:c.*100_*112del XP_006722862.1:n.*100_*112del
XM_011528133.1:c.*100_*112del XP_011526435.1:n.*100_*112del
NM_030662.4:c.*100_*112del MANE Select NP_109587.1:n.*100_*112del