Canonical Allele Identifier: CA403392369

Gene: MAP2K2

Linked Data

• dbSNP Id: rs2145079653
• MyVariant Identifiers: chr19:g.4117424G>T (hg19) ; chr19:g.4117426G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4117426G>T , CM000681.2:g.4117426G>T	GRCh38
NC_000019.9:g.4117424G>T , CM000681.1:g.4117424G>T	GRCh37
NC_000019.8:g.4068424G>T	NCBI36
NG_007996.1:g.11703C>A , LRG_750:g.11703C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.735C>A
ENST00000687128.1:n.735C>A
ENST00000262948.10:c.296C>A MANE Select	ENSP00000262948.4:p.Ala99Asp
ENST00000262948.9:c.296C>A	ENSP00000262948.3:p.Ala99Asp
ENST00000394867.8:c.5C>A	ENSP00000378336.1:p.Ala2Asp
ENST00000599345.1:n.493C>A
NM_030662.3:c.296C>A , LRG_750t1:c.296C>A	NP_109587.1:p.Ala99Asp
XM_006722799.2:c.296C>A	XP_006722862.1:p.Ala99Asp
XM_017026989.1:c.296C>A	XP_016882478.1:p.Ala99Asp
XM_017026990.1:c.296C>A	XP_016882479.1:p.Ala99Asp
XM_017026991.1:c.296C>A	XP_016882480.1:p.Ala99Asp
NM_030662.4:c.296C>A MANE Select	NP_109587.1:p.Ala99Asp