Canonical Allele Identifier: CA403392666
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4117532C>T , CM000681.2:g.4117532C>T GRCh38
NC_000019.9:g.4117530C>T , CM000681.1:g.4117530C>T GRCh37
NC_000019.8:g.4068530C>T NCBI36
NG_007996.1:g.11597G>A , LRG_750:g.11597G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.629G>A
ENST00000687128.1:n.629G>A
ENST00000262948.10:c.190G>A MANE Select ENSP00000262948.4:p.Val64Ile
ENST00000262948.9:c.190G>A ENSP00000262948.3:p.Val64Ile
ENST00000394867.8:c.-102G>A ENSP00000378336.1:n.-102G>A
ENST00000599345.1:n.387G>A
NM_030662.3:c.190G>A , LRG_750t1:c.190G>A NP_109587.1:p.Val64Ile
XM_006722799.2:c.190G>A XP_006722862.1:p.Val64Ile
XM_017026989.1:c.190G>A XP_016882478.1:p.Val64Ile
XM_017026990.1:c.190G>A XP_016882479.1:p.Val64Ile
XM_017026991.1:c.190G>A XP_016882480.1:p.Val64Ile
NM_030662.4:c.190G>A MANE Select NP_109587.1:p.Val64Ile
Search 100 bp 5'
Search 100 bp 3'