Canonical Allele Identifier: CA403387954

Gene: MAP2K2

Linked Data

• dbSNP Id: rs1348137830
• MyVariant Identifiers: chr19:g.4099405C>G (hg19) ; chr19:g.4099407C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099407C>G , CM000681.2:g.4099407C>G	GRCh38
NC_000019.9:g.4099405C>G , CM000681.1:g.4099405C>G	GRCh37
NC_000019.8:g.4050405C>G	NCBI36
NG_007996.1:g.29722G>C , LRG_750:g.29722G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1152G>C
ENST00000687128.1:n.1152G>C
ENST00000688002.1:n.1007G>C
ENST00000689792.1:n.646-29G>C
ENST00000262948.10:c.713G>C MANE Select	ENSP00000262948.4:p.Arg238Pro
ENST00000262948.9:c.713G>C	ENSP00000262948.3:p.Arg238Pro
ENST00000394867.8:c.422G>C	ENSP00000378336.1:p.Arg141Pro
ENST00000593364.5:n.660G>C
ENST00000595715.1:n.528G>C
ENST00000597263.5:n.169+1612G>C
ENST00000599021.1:c.29+1612G>C
ENST00000600584.5:n.1273G>C
ENST00000601786.5:n.1014G>C
NM_030662.3:c.713G>C , LRG_750t1:c.713G>C	NP_109587.1:p.Arg238Pro
XM_006722799.2:c.705+1612G>C	XP_006722862.1:n.705+1612G>C
XM_011528133.1:c.143G>C	XP_011526435.1:p.Arg48Pro
XM_017026989.1:c.713G>C	XP_016882478.1:p.Arg238Pro
XM_017026990.1:c.705+1612G>C	XP_016882479.1:n.705+1612G>C
NM_030662.4:c.713G>C MANE Select	NP_109587.1:p.Arg238Pro