Canonical Allele Identifier: CA403380749
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090626-G-A
MyVariant Identifiers: chr19:g.4090624G>A (hg19) chr19:g.4090626G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090626G>A , CM000681.2:g.4090626G>A GRCh38
NC_000019.9:g.4090624G>A , CM000681.1:g.4090624G>A GRCh37
NC_000019.8:g.4041624G>A NCBI36
NG_007996.1:g.38503C>T , LRG_750:g.38503C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1614C>T
ENST00000688002.1:n.3326C>T
ENST00000688751.1:n.311C>T
ENST00000689792.1:n.1079C>T
ENST00000262948.10:c.1175C>T MANE Select ENSP00000262948.4:p.Pro392Leu
ENST00000262948.9:c.1175C>T ENSP00000262948.3:p.Pro392Leu
ENST00000394867.8:c.884C>T ENSP00000378336.1:p.Pro295Leu
ENST00000597263.5:n.360C>T
ENST00000599021.1:c.285C>T
ENST00000600584.5:n.2624C>T
ENST00000601786.5:n.1476C>T
NM_030662.3:c.1175C>T , LRG_750t1:c.1175C>T NP_109587.1:p.Pro392Leu
XM_006722799.2:c.896C>T XP_006722862.1:p.Pro299Leu
XM_011528133.1:c.605C>T XP_011526435.1:p.Pro202Leu
NM_030662.4:c.1175C>T MANE Select NP_109587.1:p.Pro392Leu
Search 100 bp 5'
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