Canonical Allele Identifier: CA504984355
Gene: MAP2K2 HGNC NCBI

Linked Data

gnomAD v4: 19-4090691-C-T
MyVariant Identifiers: chr19:g.4090689C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4090691C>T , CM000681.2:g.4090691C>T GRCh38
NC_000019.9:g.4090689C>T , CM000681.1:g.4090689C>T GRCh37
NC_000019.8:g.4041689C>T NCBI36
NG_007996.1:g.38438G>A , LRG_750:g.38438G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1549G>A
ENST00000688002.1:n.3261G>A
ENST00000688751.1:n.246G>A
ENST00000689792.1:n.1014G>A
ENST00000262948.10:c.1110G>A MANE Select ENSP00000262948.4:p.Lys370=
ENST00000262948.9:c.1110G>A ENSP00000262948.3:p.Lys370=
ENST00000394867.8:c.819G>A ENSP00000378336.1:p.Lys273=
ENST00000597263.5:n.295G>A
ENST00000599021.1:c.220G>A
ENST00000600584.5:n.2559G>A
ENST00000601786.5:n.1411G>A
NM_030662.3:c.1110G>A , LRG_750t1:c.1110G>A NP_109587.1:p.Lys370=
XM_006722799.2:c.831G>A XP_006722862.1:p.Lys277=
XM_011528133.1:c.540G>A XP_011526435.1:p.Lys180=
NM_030662.4:c.1110G>A MANE Select NP_109587.1:p.Lys370=