Canonical Allele Identifier: CA2629083700
Gene: MAP2K1 HGNC NCBI

Linked Data

gnomAD v4: 15-66485328-G-GGATA
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485329_66485330insATAG , CM000677.2:g.66485329_66485330insATAG GRCh38
NC_000015.9:g.66777667_66777668insATAG , CM000677.1:g.66777667_66777668insATAG GRCh37
NC_000015.8:g.64564721_64564722insATAG NCBI36
NG_008305.1:g.103457_103458insATAG , LRG_725:g.103457_103458insATAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-1899_628-1898insATAG ENSP00000508681.1:n.628-1899_628-1898insATAG
ENST00000685172.1:c.895+138_895+139insATAG ENSP00000509604.1:n.895+138_895+139insATAG
ENST00000685763.1:c.748+138_748+139insATAG ENSP00000509016.1:n.748+138_748+139insATAG
ENST00000686347.1:c.569-1899_569-1898insATAG ENSP00000509027.1:n.569-1899_569-1898insATAG
ENST00000687191.1:n.1253+138_1253+139insATAG
ENST00000687481.1:n.310+138_310+139insATAG
ENST00000689951.1:c.946+138_946+139insATAG ENSP00000509308.1:n.946+138_946+139insATAG
ENST00000691077.1:c.*132+138_*132+139insATAG ENSP00000509843.1:n.*132+138_*132+139insATAG
ENST00000691576.1:c.766+138_766+139insATAG ENSP00000510066.1:n.766+138_766+139insATAG
ENST00000691937.1:c.895+138_895+139insATAG ENSP00000508768.1:n.895+138_895+139insATAG
ENST00000692487.1:c.*132+138_*132+139insATAG ENSP00000509534.1:n.*132+138_*132+139insATAG
ENST00000692683.1:c.829+138_829+139insATAG ENSP00000508437.1:n.829+138_829+139insATAG
ENST00000693150.1:c.751+138_751+139insATAG ENSP00000510309.1:n.751+138_751+139insATAG
ENST00000307102.10:c.895+138_895+139insATAG MANE Select ENSP00000302486.5:n.895+138_895+139insATAG
ENST00000307102.9:c.895+138_895+139insATAG ENSP00000302486.4:n.895+138_895+139insATAG
ENST00000566326.1:c.367+138_367+139insATAG ENSP00000456438.1:n.367+138_367+139insATAG
NM_002755.3:c.895+138_895+139insATAG , LRG_725t1:c.895+138_895+139insATAG NP_002746.1:n.895+138_895+139insATAG
XM_011521783.1:c.829+138_829+139insATAG XP_011520085.1:n.829+138_829+139insATAG
XM_011521783.3:c.829+138_829+139insATAG XP_011520085.1:n.829+138_829+139insATAG
XM_017022411.2:c.817+138_817+139insATAG XP_016877900.1:n.817+138_817+139insATAG
XM_017022412.1:c.751+138_751+139insATAG XP_016877901.1:n.751+138_751+139insATAG
XM_017022413.1:c.367+138_367+139insATAG XP_016877902.1:n.367+138_367+139insATAG
NM_002755.4:c.895+138_895+139insATAG MANE Select NP_002746.1:n.895+138_895+139insATAG
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