Canonical Allele Identifier: CA882241154
Gene: MAP2K2 HGNC NCBI

Linked Data

dbSNP Id: rs1491183505

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090338_4090339insTT , CM000681.2:g.4090338_4090339insTT GRCh38
NC_000019.9:g.4090336_4090337insTT , CM000681.1:g.4090336_4090337insTT GRCh37
NC_000019.8:g.4041336_4041337insTT NCBI36
NG_007996.1:g.38791_38792insAA , LRG_750:g.38791_38792insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000689792.1:n.1367_1368insAA
ENST00000262948.10:c.*260_*261insAA MANE Select ENSP00000262948.4:n.*260_*261insAA
ENST00000262948.9:c.*260_*261insAA ENSP00000262948.3:n.*260_*261insAA
ENST00000394867.8:c.*260_*261insAA ENSP00000378336.1:n.*260_*261insAA
ENST00000600584.5:n.2912_2913insAA
ENST00000601786.5:n.1764_1765insAA
NM_030662.3:c.*260_*261insAA , LRG_750t1:c.*260_*261insAA NP_109587.1:n.*260_*261insAA
XM_006722799.2:c.*260_*261insAA XP_006722862.1:n.*260_*261insAA
XM_011528133.1:c.*260_*261insAA XP_011526435.1:n.*260_*261insAA
NM_030662.4:c.*260_*261insAA MANE Select NP_109587.1:n.*260_*261insAA