Canonical Allele Identifier: CA403380588

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4090598A>G (hg19) ; chr19:g.4090600A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090600A>G , CM000681.2:g.4090600A>G	GRCh38
NC_000019.9:g.4090598A>G , CM000681.1:g.4090598A>G	GRCh37
NC_000019.8:g.4041598A>G	NCBI36
NG_007996.1:g.38529T>C , LRG_750:g.38529T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1640T>C
ENST00000688002.1:n.3352T>C
ENST00000688751.1:n.337T>C
ENST00000689792.1:n.1105T>C
ENST00000262948.10:c.1201T>C MANE Select	ENSP00000262948.4:p.Ter401Arg
ENST00000262948.9:c.1201T>C	ENSP00000262948.3:p.Ter401Arg
ENST00000394867.8:c.910T>C	ENSP00000378336.1:p.Ter304Arg
ENST00000597263.5:n.386T>C
ENST00000599021.1:c.311T>C
ENST00000600584.5:n.2650T>C
ENST00000601786.5:n.1502T>C
NM_030662.3:c.1201T>C , LRG_750t1:c.1201T>C	NP_109587.1:p.Ter401Arg
XM_006722799.2:c.922T>C	XP_006722862.1:p.Ter308Arg
XM_011528133.1:c.631T>C	XP_011526435.1:p.Ter211Arg
NM_030662.4:c.1201T>C MANE Select	NP_109587.1:p.Ter401Arg