Canonical Allele Identifier: CA403380699
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090616G>T (hg19) chr19:g.4090618G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090618G>T , CM000681.2:g.4090618G>T GRCh38
NC_000019.9:g.4090616G>T , CM000681.1:g.4090616G>T GRCh37
NC_000019.8:g.4041616G>T NCBI36
NG_007996.1:g.38511C>A , LRG_750:g.38511C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1622C>A
ENST00000688002.1:n.3334C>A
ENST00000688751.1:n.319C>A
ENST00000689792.1:n.1087C>A
ENST00000262948.10:c.1183C>A MANE Select ENSP00000262948.4:p.Pro395Thr
ENST00000262948.9:c.1183C>A ENSP00000262948.3:p.Pro395Thr
ENST00000394867.8:c.892C>A ENSP00000378336.1:p.Pro298Thr
ENST00000597263.5:n.368C>A
ENST00000599021.1:c.293C>A
ENST00000600584.5:n.2632C>A
ENST00000601786.5:n.1484C>A
NM_030662.3:c.1183C>A , LRG_750t1:c.1183C>A NP_109587.1:p.Pro395Thr
XM_006722799.2:c.904C>A XP_006722862.1:p.Pro302Thr
XM_011528133.1:c.613C>A XP_011526435.1:p.Pro205Thr
NM_030662.4:c.1183C>A MANE Select NP_109587.1:p.Pro395Thr
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