Canonical Allele Identifier: CA992817193
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs2040842931

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090363_4090366dup , CM000681.2:g.4090363_4090366dup GRCh38
NC_000019.9:g.4090361_4090364dup , CM000681.1:g.4090361_4090364dup GRCh37
NC_000019.8:g.4041361_4041364dup NCBI36
NG_007996.1:g.38763_38766dup , LRG_750:g.38763_38766dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1874_1877dup
ENST00000688751.1:n.571_574dup
ENST00000689792.1:n.1339_1342dup
ENST00000262948.10:c.*232_*235dup MANE Select ENSP00000262948.4:n.*232_*235dup
ENST00000262948.9:c.*232_*235dup ENSP00000262948.3:n.*232_*235dup
ENST00000394867.8:c.*232_*235dup ENSP00000378336.1:n.*232_*235dup
ENST00000600584.5:n.2884_2887dup
ENST00000601786.5:n.1736_1739dup
NM_030662.3:c.*232_*235dup , LRG_750t1:c.*232_*235dup NP_109587.1:n.*232_*235dup
XM_006722799.2:c.*232_*235dup XP_006722862.1:n.*232_*235dup
XM_011528133.1:c.*232_*235dup XP_011526435.1:n.*232_*235dup
NM_030662.4:c.*232_*235dup MANE Select NP_109587.1:n.*232_*235dup