Canonical Allele Identifier: CA403380817
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090633A>T (hg19) chr19:g.4090635A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090635A>T , CM000681.2:g.4090635A>T GRCh38
NC_000019.9:g.4090633A>T , CM000681.1:g.4090633A>T GRCh37
NC_000019.8:g.4041633A>T NCBI36
NG_007996.1:g.38494T>A , LRG_750:g.38494T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1605T>A
ENST00000688002.1:n.3317T>A
ENST00000688751.1:n.302T>A
ENST00000689792.1:n.1070T>A
ENST00000262948.10:c.1166T>A MANE Select ENSP00000262948.4:p.Leu389Gln
ENST00000262948.9:c.1166T>A ENSP00000262948.3:p.Leu389Gln
ENST00000394867.8:c.875T>A ENSP00000378336.1:p.Leu292Gln
ENST00000597263.5:n.351T>A
ENST00000599021.1:c.276T>A
ENST00000600584.5:n.2615T>A
ENST00000601786.5:n.1467T>A
NM_030662.3:c.1166T>A , LRG_750t1:c.1166T>A NP_109587.1:p.Leu389Gln
XM_006722799.2:c.887T>A XP_006722862.1:p.Leu296Gln
XM_011528133.1:c.596T>A XP_011526435.1:p.Leu199Gln
NM_030662.4:c.1166T>A MANE Select NP_109587.1:p.Leu389Gln
Search 100 bp 5'
Search 100 bp 3'