Canonical Allele Identifier: CA403387856

Gene: MAP2K2

Linked Data

• ClinVar Variation Id: 2231900
• ClinVar RCV Id: RCV004093927
• gnomAD v4: 19-4099393-G-T
• MyVariant Identifiers: chr19:g.4099391G>T (hg19) ; chr19:g.4099393G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099393G>T , CM000681.2:g.4099393G>T	GRCh38
NC_000019.9:g.4099391G>T , CM000681.1:g.4099391G>T	GRCh37
NC_000019.8:g.4050391G>T	NCBI36
NG_007996.1:g.29736C>A , LRG_750:g.29736C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1166C>A
ENST00000687128.1:n.1166C>A
ENST00000688002.1:n.1021C>A
ENST00000689792.1:n.646-15C>A
ENST00000262948.10:c.727C>A MANE Select	ENSP00000262948.4:p.His243Asn
ENST00000262948.9:c.727C>A	ENSP00000262948.3:p.His243Asn
ENST00000394867.8:c.436C>A	ENSP00000378336.1:p.His146Asn
ENST00000593364.5:n.674C>A
ENST00000595715.1:n.542C>A
ENST00000597263.5:n.169+1626C>A
ENST00000599021.1:c.29+1626C>A
ENST00000600584.5:n.1287C>A
ENST00000601786.5:n.1028C>A
NM_030662.3:c.727C>A , LRG_750t1:c.727C>A	NP_109587.1:p.His243Asn
XM_006722799.2:c.705+1626C>A	XP_006722862.1:n.705+1626C>A
XM_011528133.1:c.157C>A	XP_011526435.1:p.His53Asn
XM_017026989.1:c.727C>A	XP_016882478.1:p.His243Asn
XM_017026990.1:c.705+1626C>A	XP_016882479.1:n.705+1626C>A
NM_030662.4:c.727C>A MANE Select	NP_109587.1:p.His243Asn