Canonical Allele Identifier: CA2184071775
Gene: MAP2K1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66435213_66435218delinsTTCTGG , CM000677.2:g.66435213_66435218delinsTTCTGG GRCh38
NC_000015.9:g.66727551_66727556delinsTTCTGG , CM000677.1:g.66727551_66727556delinsTTCTGG GRCh37
NC_000015.8:g.64514605_64514610delinsTTCTGG NCBI36
NG_008305.1:g.53341_53346delinsTTCTGG , LRG_725:g.53341_53346delinsTTCTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.201_206delinsTTCTGG ENSP00000508681.1:p.Pro67=
ENST00000685172.1:c.267_272delinsTTCTGG ENSP00000509604.1:p.Pro89=
ENST00000685763.1:c.267_272delinsTTCTGG ENSP00000509016.1:p.Pro89=
ENST00000686347.1:c.267_272delinsTTCTGG ENSP00000509027.1:p.Pro89=
ENST00000687191.1:n.703_708delinsTTCTGG
ENST00000689951.1:c.267_272delinsTTCTGG ENSP00000509308.1:p.Pro89=
ENST00000691077.1:c.267_272delinsTTCTGG ENSP00000509843.1:p.Pro89=
ENST00000691576.1:c.267_272delinsTTCTGG ENSP00000510066.1:p.Pro89=
ENST00000691937.1:c.267_272delinsTTCTGG ENSP00000508768.1:p.Pro89=
ENST00000692487.1:c.267_272delinsTTCTGG ENSP00000509534.1:p.Pro89=
ENST00000692683.1:c.201_206delinsTTCTGG ENSP00000508437.1:p.Pro67=
ENST00000693150.1:c.201_206delinsTTCTGG ENSP00000510309.1:p.Pro67=
ENST00000307102.10:c.267_272delinsTTCTGG MANE Select ENSP00000302486.5:p.Pro89=
ENST00000307102.9:c.267_272delinsTTCTGG ENSP00000302486.4:p.Pro89=
ENST00000425818.2:n.778_783delinsTTCTGG
NM_002755.3:c.267_272delinsTTCTGG , LRG_725t1:c.267_272delinsTTCTGG NP_002746.1:p.Pro89=
XM_011521783.1:c.201_206delinsTTCTGG XP_011520085.1:p.Pro67=
XM_011521783.3:c.201_206delinsTTCTGG XP_011520085.1:p.Pro67=
XM_017022411.2:c.267_272delinsTTCTGG XP_016877900.1:p.Pro89=
XM_017022412.1:c.201_206delinsTTCTGG XP_016877901.1:p.Pro67=
NM_002755.4:c.267_272delinsTTCTGG MANE Select NP_002746.1:p.Pro89=
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