Canonical Allele Identifier: CA403387821

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4099387T>G (hg19) ; chr19:g.4099389T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099389T>G , CM000681.2:g.4099389T>G	GRCh38
NC_000019.9:g.4099387T>G , CM000681.1:g.4099387T>G	GRCh37
NC_000019.8:g.4050387T>G	NCBI36
NG_007996.1:g.29740A>C , LRG_750:g.29740A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1170A>C
ENST00000687128.1:n.1170A>C
ENST00000688002.1:n.1025A>C
ENST00000689792.1:n.646-11A>C
ENST00000262948.10:c.731A>C MANE Select	ENSP00000262948.4:p.Tyr244Ser
ENST00000262948.9:c.731A>C	ENSP00000262948.3:p.Tyr244Ser
ENST00000394867.8:c.440A>C	ENSP00000378336.1:p.Tyr147Ser
ENST00000593364.5:n.678A>C
ENST00000595715.1:n.546A>C
ENST00000597263.5:n.169+1630A>C
ENST00000599021.1:c.29+1630A>C
ENST00000600584.5:n.1291A>C
ENST00000601786.5:n.1032A>C
NM_030662.3:c.731A>C , LRG_750t1:c.731A>C	NP_109587.1:p.Tyr244Ser
XM_006722799.2:c.705+1630A>C	XP_006722862.1:n.705+1630A>C
XM_011528133.1:c.161A>C	XP_011526435.1:p.Tyr54Ser
XM_017026989.1:c.731A>C	XP_016882478.1:p.Tyr244Ser
XM_017026990.1:c.705+1630A>C	XP_016882479.1:n.705+1630A>C
NM_030662.4:c.731A>C MANE Select	NP_109587.1:p.Tyr244Ser