Canonical Allele Identifier: CA403381212
Gene: MAP2K2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.4090697A>G (hg19) chr19:g.4090699A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090699A>G , CM000681.2:g.4090699A>G GRCh38
NC_000019.9:g.4090697A>G , CM000681.1:g.4090697A>G GRCh37
NC_000019.8:g.4041697A>G NCBI36
NG_007996.1:g.38430T>C , LRG_750:g.38430T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1541T>C
ENST00000688002.1:n.3253T>C
ENST00000688751.1:n.238T>C
ENST00000689792.1:n.1006T>C
ENST00000262948.10:c.1102T>C MANE Select ENSP00000262948.4:p.Phe368Leu
ENST00000262948.9:c.1102T>C ENSP00000262948.3:p.Phe368Leu
ENST00000394867.8:c.811T>C ENSP00000378336.1:p.Phe271Leu
ENST00000597263.5:n.287T>C
ENST00000599021.1:c.212T>C
ENST00000600584.5:n.2551T>C
ENST00000601786.5:n.1403T>C
NM_030662.3:c.1102T>C , LRG_750t1:c.1102T>C NP_109587.1:p.Phe368Leu
XM_006722799.2:c.823T>C XP_006722862.1:p.Phe275Leu
XM_011528133.1:c.532T>C XP_011526435.1:p.Phe178Leu
NM_030662.4:c.1102T>C MANE Select NP_109587.1:p.Phe368Leu
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