Canonical Allele Identifier: CA504986745

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4099311C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099313C>G , CM000681.2:g.4099313C>G	GRCh38
NC_000019.9:g.4099311C>G , CM000681.1:g.4099311C>G	GRCh37
NC_000019.8:g.4050311C>G	NCBI36
NG_007996.1:g.29816G>C , LRG_750:g.29816G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1246G>C
ENST00000687128.1:n.1246G>C
ENST00000688002.1:n.1101G>C
ENST00000689792.1:n.711G>C
ENST00000262948.10:c.807G>C MANE Select	ENSP00000262948.4:p.Pro269=
ENST00000262948.9:c.807G>C	ENSP00000262948.3:p.Pro269=
ENST00000394867.8:c.516G>C	ENSP00000378336.1:p.Pro172=
ENST00000593364.5:n.754G>C
ENST00000595715.1:n.622G>C
ENST00000597263.5:n.169+1706G>C
ENST00000599021.1:c.29+1706G>C
ENST00000600584.5:n.1367G>C
ENST00000601786.5:n.1108G>C
NM_030662.3:c.807G>C , LRG_750t1:c.807G>C	NP_109587.1:p.Pro269=
XM_006722799.2:c.705+1706G>C	XP_006722862.1:n.705+1706G>C
XM_011528133.1:c.237G>C	XP_011526435.1:p.Pro79=
XM_017026989.1:c.807G>C	XP_016882478.1:p.Pro269=
XM_017026990.1:c.705+1706G>C	XP_016882479.1:n.705+1706G>C
NM_030662.4:c.807G>C MANE Select	NP_109587.1:p.Pro269=