Canonical Allele Identifier: CA2319230434
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4109908_4109911delinsACCC , CM000681.2:g.4109908_4109911delinsACCC GRCh38
NC_000019.9:g.4109906_4109909delinsACCC , CM000681.1:g.4109906_4109909delinsACCC GRCh37
NC_000019.8:g.4060906_4060909delinsACCC NCBI36
NG_007996.1:g.19218_19221delinsGGGT , LRG_750:g.19218_19221delinsGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.889+598_889+601delinsGGGT
ENST00000687128.1:n.889+598_889+601delinsGGGT
ENST00000262948.10:c.450+598_450+601delinsGGGT MANE Select ENSP00000262948.4:n.450+598_450+601delinsGGGT
ENST00000262948.9:c.450+598_450+601delinsGGGT ENSP00000262948.3:n.450+598_450+601delinsGGGT
ENST00000394867.8:c.159+598_159+601delinsGGGT ENSP00000378336.1:n.159+598_159+601delinsGGGT
ENST00000599345.1:n.647+598_647+601delinsGGGT
NM_030662.3:c.450+598_450+601delinsGGGT , LRG_750t1:c.450+598_450+601delinsGGGT NP_109587.1:n.450+598_450+601delinsGGGT
XM_006722799.2:c.450+598_450+601delinsGGGT XP_006722862.1:n.450+598_450+601delinsGGGT
XM_017026989.1:c.450+598_450+601delinsGGGT XP_016882478.1:n.450+598_450+601delinsGGGT
XM_017026990.1:c.450+598_450+601delinsGGGT XP_016882479.1:n.450+598_450+601delinsGGGT
XM_017026991.1:c.450+598_450+601delinsGGGT XP_016882480.1:n.450+598_450+601delinsGGGT
NM_030662.4:c.450+598_450+601delinsGGGT MANE Select NP_109587.1:n.450+598_450+601delinsGGGT
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