Canonical Allele Identifier: CA2584876597
Gene: MAP2K2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090522_4090526del , CM000681.2:g.4090522_4090526del GRCh38
NC_000019.9:g.4090520_4090524del , CM000681.1:g.4090520_4090524del GRCh37
NC_000019.8:g.4041520_4041524del NCBI36
NG_007996.1:g.38603_38607del , LRG_750:g.38603_38607del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1714_1718del
ENST00000688002.1:n.3426_3430del
ENST00000688751.1:n.411_415del
ENST00000689792.1:n.1179_1183del
ENST00000262948.10:c.*72_*76del MANE Select ENSP00000262948.4:n.*72_*76del
ENST00000262948.9:c.*72_*76del ENSP00000262948.3:n.*72_*76del
ENST00000394867.8:c.*72_*76del ENSP00000378336.1:n.*72_*76del
ENST00000597263.5:n.460_464del
ENST00000600584.5:n.2724_2728del
ENST00000601786.5:n.1576_1580del
NM_030662.3:c.*72_*76del , LRG_750t1:c.*72_*76del NP_109587.1:n.*72_*76del
XM_006722799.2:c.*72_*76del XP_006722862.1:n.*72_*76del
XM_011528133.1:c.*72_*76del XP_011526435.1:n.*72_*76del
NM_030662.4:c.*72_*76del MANE Select NP_109587.1:n.*72_*76del