Canonical Allele Identifier: CA2629083705
Gene: MAP2K1 HGNC NCBI

Linked Data

gnomAD v4: 15-66485331-A-ACTT
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.66485331_66485332insCTT , CM000677.2:g.66485331_66485332insCTT GRCh38
NC_000015.9:g.66777669_66777670insCTT , CM000677.1:g.66777669_66777670insCTT GRCh37
NC_000015.8:g.64564723_64564724insCTT NCBI36
NG_008305.1:g.103459_103460insCTT , LRG_725:g.103459_103460insCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000684779.1:c.628-1897_628-1896insCTT ENSP00000508681.1:n.628-1897_628-1896insCTT
ENST00000685172.1:c.895+140_895+141insCTT ENSP00000509604.1:n.895+140_895+141insCTT
ENST00000685763.1:c.748+140_748+141insCTT ENSP00000509016.1:n.748+140_748+141insCTT
ENST00000686347.1:c.569-1897_569-1896insCTT ENSP00000509027.1:n.569-1897_569-1896insCTT
ENST00000687191.1:n.1253+140_1253+141insCTT
ENST00000687481.1:n.310+140_310+141insCTT
ENST00000689951.1:c.946+140_946+141insCTT ENSP00000509308.1:n.946+140_946+141insCTT
ENST00000691077.1:c.*132+140_*132+141insCTT ENSP00000509843.1:n.*132+140_*132+141insCTT
ENST00000691576.1:c.766+140_766+141insCTT ENSP00000510066.1:n.766+140_766+141insCTT
ENST00000691937.1:c.895+140_895+141insCTT ENSP00000508768.1:n.895+140_895+141insCTT
ENST00000692487.1:c.*132+140_*132+141insCTT ENSP00000509534.1:n.*132+140_*132+141insCTT
ENST00000692683.1:c.829+140_829+141insCTT ENSP00000508437.1:n.829+140_829+141insCTT
ENST00000693150.1:c.751+140_751+141insCTT ENSP00000510309.1:n.751+140_751+141insCTT
ENST00000307102.10:c.895+140_895+141insCTT MANE Select ENSP00000302486.5:n.895+140_895+141insCTT
ENST00000307102.9:c.895+140_895+141insCTT ENSP00000302486.4:n.895+140_895+141insCTT
ENST00000566326.1:c.367+140_367+141insCTT ENSP00000456438.1:n.367+140_367+141insCTT
NM_002755.3:c.895+140_895+141insCTT , LRG_725t1:c.895+140_895+141insCTT NP_002746.1:n.895+140_895+141insCTT
XM_011521783.1:c.829+140_829+141insCTT XP_011520085.1:n.829+140_829+141insCTT
XM_011521783.3:c.829+140_829+141insCTT XP_011520085.1:n.829+140_829+141insCTT
XM_017022411.2:c.817+140_817+141insCTT XP_016877900.1:n.817+140_817+141insCTT
XM_017022412.1:c.751+140_751+141insCTT XP_016877901.1:n.751+140_751+141insCTT
XM_017022413.1:c.367+140_367+141insCTT XP_016877902.1:n.367+140_367+141insCTT
NM_002755.4:c.895+140_895+141insCTT MANE Select NP_002746.1:n.895+140_895+141insCTT
Search 100 bp 5'
Search 100 bp 3'