Canonical Allele Identifier: CA2319219629
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090439C= , CM000681.2:g.4090439C= GRCh38
NC_000019.9:g.4090437C= , CM000681.1:g.4090437C= GRCh37
NC_000019.8:g.4041437C= NCBI36
NG_007996.1:g.38690G= , LRG_750:g.38690G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1801G=
ENST00000688751.1:n.498G=
ENST00000689792.1:n.1266G=
ENST00000262948.10:c.*159G= MANE Select ENSP00000262948.4:n.*159G=
ENST00000262948.9:c.*159G= ENSP00000262948.3:n.*159G=
ENST00000394867.8:c.*159G= ENSP00000378336.1:n.*159G=
ENST00000597263.5:n.547G=
ENST00000600584.5:n.2811G=
ENST00000601786.5:n.1663G=
NM_030662.3:c.*159G= , LRG_750t1:c.*159G= NP_109587.1:n.*159G=
XM_006722799.2:c.*159G= XP_006722862.1:n.*159G=
XM_011528133.1:c.*159G= XP_011526435.1:n.*159G=
NM_030662.4:c.*159G= MANE Select NP_109587.1:n.*159G=
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