Canonical Allele Identifier: CA920042899
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4109912_4109914del , CM000681.2:g.4109912_4109914del GRCh38
NC_000019.9:g.4109910_4109912del , CM000681.1:g.4109910_4109912del GRCh37
NC_000019.8:g.4060910_4060912del NCBI36
NG_007996.1:g.19218_19220del , LRG_750:g.19218_19220del

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.889+598_889+600del
ENST00000687128.1:n.889+598_889+600del
ENST00000262948.10:c.450+598_450+600del MANE Select ENSP00000262948.4:n.450+598_450+600del
ENST00000262948.9:c.450+598_450+600del ENSP00000262948.3:n.450+598_450+600del
ENST00000394867.8:c.159+598_159+600del ENSP00000378336.1:n.159+598_159+600del
ENST00000599345.1:n.647+598_647+600del
NM_030662.3:c.450+598_450+600del , LRG_750t1:c.450+598_450+600del NP_109587.1:n.450+598_450+600del
XM_006722799.2:c.450+598_450+600del XP_006722862.1:n.450+598_450+600del
XM_017026989.1:c.450+598_450+600del XP_016882478.1:n.450+598_450+600del
XM_017026990.1:c.450+598_450+600del XP_016882479.1:n.450+598_450+600del
XM_017026991.1:c.450+598_450+600del XP_016882480.1:n.450+598_450+600del
NM_030662.4:c.450+598_450+600del MANE Select NP_109587.1:n.450+598_450+600del
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