Canonical Allele Identifier: CA403391758

Gene: MAP2K2

Linked Data

• ClinVar Variation Id: 2442537
• ClinVar RCV Id: RCV003149309
• MyVariant Identifiers: chr19:g.4110640T>G (hg19) ; chr19:g.4110642T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4110642T>G , CM000681.2:g.4110642T>G	GRCh38
NC_000019.9:g.4110640T>G , CM000681.1:g.4110640T>G	GRCh37
NC_000019.8:g.4061640T>G	NCBI36
NG_007996.1:g.18487A>C , LRG_750:g.18487A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.756A>C
ENST00000687128.1:n.756A>C
ENST00000262948.10:c.317A>C MANE Select	ENSP00000262948.4:p.Glu106Ala
ENST00000262948.9:c.317A>C	ENSP00000262948.3:p.Glu106Ala
ENST00000394867.8:c.26A>C	ENSP00000378336.1:p.Glu9Ala
ENST00000599345.1:n.514A>C
NM_030662.3:c.317A>C , LRG_750t1:c.317A>C	NP_109587.1:p.Glu106Ala
XM_006722799.2:c.317A>C	XP_006722862.1:p.Glu106Ala
XM_017026989.1:c.317A>C	XP_016882478.1:p.Glu106Ala
XM_017026990.1:c.317A>C	XP_016882479.1:p.Glu106Ala
XM_017026991.1:c.317A>C	XP_016882480.1:p.Glu106Ala
NM_030662.4:c.317A>C MANE Select	NP_109587.1:p.Glu106Ala