Canonical Allele Identifier: CA403380664

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4090610G>T (hg19) ; chr19:g.4090612G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090612G>T , CM000681.2:g.4090612G>T	GRCh38
NC_000019.9:g.4090610G>T , CM000681.1:g.4090610G>T	GRCh37
NC_000019.8:g.4041610G>T	NCBI36
NG_007996.1:g.38517C>A , LRG_750:g.38517C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1628C>A
ENST00000688002.1:n.3340C>A
ENST00000688751.1:n.325C>A
ENST00000689792.1:n.1093C>A
ENST00000262948.10:c.1189C>A MANE Select	ENSP00000262948.4:p.Arg397Ser
ENST00000262948.9:c.1189C>A	ENSP00000262948.3:p.Arg397Ser
ENST00000394867.8:c.898C>A	ENSP00000378336.1:p.Arg300Ser
ENST00000597263.5:n.374C>A
ENST00000599021.1:c.299C>A
ENST00000600584.5:n.2638C>A
ENST00000601786.5:n.1490C>A
NM_030662.3:c.1189C>A , LRG_750t1:c.1189C>A	NP_109587.1:p.Arg397Ser
XM_006722799.2:c.910C>A	XP_006722862.1:p.Arg304Ser
XM_011528133.1:c.619C>A	XP_011526435.1:p.Arg207Ser
NM_030662.4:c.1189C>A MANE Select	NP_109587.1:p.Arg397Ser