Canonical Allele Identifier: CA403385132

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099207-C-A
• MyVariant Identifiers: chr19:g.4099205C>A (hg19) ; chr19:g.4099207C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099207C>A , CM000681.2:g.4099207C>A	GRCh38
NC_000019.9:g.4099205C>A , CM000681.1:g.4099205C>A	GRCh37
NC_000019.8:g.4050205C>A	NCBI36
NG_007996.1:g.29922G>T , LRG_750:g.29922G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000394867.9:n.1352G>T
ENST00000687128.1:n.1352G>T
ENST00000688002.1:n.1207G>T
ENST00000689792.1:n.817G>T
ENST00000262948.10:c.913G>T MANE Select	ENSP00000262948.4:p.Val305Phe
ENST00000262948.9:c.913G>T	ENSP00000262948.3:p.Val305Phe
ENST00000394867.8:c.622G>T	ENSP00000378336.1:p.Val208Phe
ENST00000593364.5:n.860G>T
ENST00000595715.1:n.728G>T
ENST00000597263.5:n.169+1812G>T
ENST00000599021.1:c.29+1812G>T
ENST00000600584.5:n.1473G>T
ENST00000601786.5:n.1214G>T
NM_030662.3:c.913G>T , LRG_750t1:c.913G>T	NP_109587.1:p.Val305Phe
XM_006722799.2:c.705+1812G>T	XP_006722862.1:n.705+1812G>T
XM_011528133.1:c.343G>T	XP_011526435.1:p.Val115Phe
XM_017026989.1:c.913G>T	XP_016882478.1:p.Val305Phe
XM_017026990.1:c.705+1812G>T	XP_016882479.1:n.705+1812G>T
NM_030662.4:c.913G>T MANE Select	NP_109587.1:p.Val305Phe