Canonical Allele Identifier: CA403383091

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4095386C>G (hg19) ; chr19:g.4095388C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095388C>G , CM000681.2:g.4095388C>G	GRCh38
NC_000019.9:g.4095386C>G , CM000681.1:g.4095386C>G	GRCh37
NC_000019.8:g.4046386C>G	NCBI36
NG_007996.1:g.33741G>C , LRG_750:g.33741G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1485G>C
ENST00000688002.1:n.3197G>C
ENST00000688751.1:n.182G>C
ENST00000689792.1:n.950G>C
ENST00000262948.10:c.1046G>C MANE Select	ENSP00000262948.4:p.Cys349Ser
ENST00000262948.9:c.1046G>C	ENSP00000262948.3:p.Cys349Ser
ENST00000394867.8:c.755G>C	ENSP00000378336.1:p.Cys252Ser
ENST00000595715.1:n.861G>C
ENST00000597263.5:n.231G>C
ENST00000599021.1:c.156G>C
ENST00000600584.5:n.1606G>C
ENST00000601786.5:n.1347G>C
NM_030662.3:c.1046G>C , LRG_750t1:c.1046G>C	NP_109587.1:p.Cys349Ser
XM_006722799.2:c.767G>C	XP_006722862.1:p.Cys256Ser
XM_011528133.1:c.476G>C	XP_011526435.1:p.Cys159Ser
XM_017026989.1:c.1046G>C	XP_016882478.1:p.Trp349Ser
XM_017026990.1:c.767G>C	XP_016882479.1:p.Trp256Ser
NM_030662.4:c.1046G>C MANE Select	NP_109587.1:p.Cys349Ser