Canonical Allele Identifier: CA403380821
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090636-G-T
MyVariant Identifiers: chr19:g.4090634G>T (hg19) chr19:g.4090636G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090636G>T , CM000681.2:g.4090636G>T GRCh38
NC_000019.9:g.4090634G>T , CM000681.1:g.4090634G>T GRCh37
NC_000019.8:g.4041634G>T NCBI36
NG_007996.1:g.38493C>A , LRG_750:g.38493C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1604C>A
ENST00000688002.1:n.3316C>A
ENST00000688751.1:n.301C>A
ENST00000689792.1:n.1069C>A
ENST00000262948.10:c.1165C>A MANE Select ENSP00000262948.4:p.Leu389Met
ENST00000262948.9:c.1165C>A ENSP00000262948.3:p.Leu389Met
ENST00000394867.8:c.874C>A ENSP00000378336.1:p.Leu292Met
ENST00000597263.5:n.350C>A
ENST00000599021.1:c.275C>A
ENST00000600584.5:n.2614C>A
ENST00000601786.5:n.1466C>A
NM_030662.3:c.1165C>A , LRG_750t1:c.1165C>A NP_109587.1:p.Leu389Met
XM_006722799.2:c.886C>A XP_006722862.1:p.Leu296Met
XM_011528133.1:c.595C>A XP_011526435.1:p.Leu199Met
NM_030662.4:c.1165C>A MANE Select NP_109587.1:p.Leu389Met
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