Canonical Allele Identifier: CA2184097457
Gene: MAP2K1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66481848_66481851delinsACTC , CM000677.2:g.66481848_66481851delinsACTC GRCh38
NC_000015.9:g.66774186_66774189delinsACTC , CM000677.1:g.66774186_66774189delinsACTC GRCh37
NC_000015.8:g.64561240_64561243delinsACTC NCBI36
NG_008305.1:g.99976_99979delinsACTC , LRG_725:g.99976_99979delinsACTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.596_599delinsACTC ENSP00000508681.1:p.Asn199=
ENST00000685172.1:c.662_665delinsACTC ENSP00000509604.1:p.Asn221=
ENST00000685763.1:c.515_518delinsACTC ENSP00000509016.1:p.Asn172=
ENST00000686347.1:c.569-5380_569-5377delinsACTC ENSP00000509027.1:n.569-5380_569-5377delinsACTC
ENST00000687191.1:n.1020_1023delinsACTC
ENST00000689951.1:c.713_716delinsACTC ENSP00000509308.1:p.Asn238=
ENST00000691077.1:c.662_665delinsACTC ENSP00000509843.1:p.Asn221=
ENST00000691576.1:c.569-3146_569-3143delinsACTC ENSP00000510066.1:n.569-3146_569-3143delinsACTC
ENST00000691937.1:c.662_665delinsACTC ENSP00000508768.1:p.Asn221=
ENST00000692487.1:c.662_665delinsACTC ENSP00000509534.1:p.Asn221=
ENST00000692683.1:c.596_599delinsACTC ENSP00000508437.1:p.Asn199=
ENST00000693150.1:c.518_521delinsACTC ENSP00000510309.1:p.Asn173=
ENST00000307102.10:c.662_665delinsACTC MANE Select ENSP00000302486.5:p.Asn221=
ENST00000307102.9:c.662_665delinsACTC ENSP00000302486.4:p.Asn221=
ENST00000566326.1:c.134_137delinsACTC ENSP00000456438.1:p.Asn45=
NM_002755.3:c.662_665delinsACTC , LRG_725t1:c.662_665delinsACTC NP_002746.1:p.Asn221=
XM_011521783.1:c.596_599delinsACTC XP_011520085.1:p.Asn199=
XM_011521783.3:c.596_599delinsACTC XP_011520085.1:p.Asn199=
XM_017022411.2:c.584_587delinsACTC XP_016877900.1:p.Asn195=
XM_017022412.1:c.518_521delinsACTC XP_016877901.1:p.Asn173=
XM_017022413.1:c.134_137delinsACTC XP_016877902.1:p.Asn45=
NM_002755.4:c.662_665delinsACTC MANE Select NP_002746.1:p.Asn221=
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