Canonical Allele Identifier: CA403380646

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4090607T>A (hg19) ; chr19:g.4090609T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090609T>A , CM000681.2:g.4090609T>A	GRCh38
NC_000019.9:g.4090607T>A , CM000681.1:g.4090607T>A	GRCh37
NC_000019.8:g.4041607T>A	NCBI36
NG_007996.1:g.38520A>T , LRG_750:g.38520A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1631A>T
ENST00000688002.1:n.3343A>T
ENST00000688751.1:n.328A>T
ENST00000689792.1:n.1096A>T
ENST00000262948.10:c.1192A>T MANE Select	ENSP00000262948.4:p.Thr398Ser
ENST00000262948.9:c.1192A>T	ENSP00000262948.3:p.Thr398Ser
ENST00000394867.8:c.901A>T	ENSP00000378336.1:p.Thr301Ser
ENST00000597263.5:n.377A>T
ENST00000599021.1:c.302A>T
ENST00000600584.5:n.2641A>T
ENST00000601786.5:n.1493A>T
NM_030662.3:c.1192A>T , LRG_750t1:c.1192A>T	NP_109587.1:p.Thr398Ser
XM_006722799.2:c.913A>T	XP_006722862.1:p.Thr305Ser
XM_011528133.1:c.622A>T	XP_011526435.1:p.Thr208Ser
NM_030662.4:c.1192A>T MANE Select	NP_109587.1:p.Thr398Ser