Canonical Allele Identifier: CA504987053

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4099412-C-G
• MyVariant Identifiers: chr19:g.4099410C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099412C>G , CM000681.2:g.4099412C>G	GRCh38
NC_000019.9:g.4099410C>G , CM000681.1:g.4099410C>G	GRCh37
NC_000019.8:g.4050410C>G	NCBI36
NG_007996.1:g.29717G>C , LRG_750:g.29717G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1147G>C
ENST00000687128.1:n.1147G>C
ENST00000688002.1:n.1002G>C
ENST00000689792.1:n.646-34G>C
ENST00000262948.10:c.708G>C MANE Select	ENSP00000262948.4:p.Pro236=
ENST00000262948.9:c.708G>C	ENSP00000262948.3:p.Pro236=
ENST00000394867.8:c.417G>C	ENSP00000378336.1:p.Pro139=
ENST00000593364.5:n.655G>C
ENST00000595715.1:n.523G>C
ENST00000597263.5:n.169+1607G>C
ENST00000599021.1:c.29+1607G>C
ENST00000600584.5:n.1268G>C
ENST00000601786.5:n.1009G>C
ENST00000602167.5:n.428G>C
NM_030662.3:c.708G>C , LRG_750t1:c.708G>C	NP_109587.1:p.Pro236=
XM_006722799.2:c.705+1607G>C	XP_006722862.1:n.705+1607G>C
XM_011528133.1:c.138G>C	XP_011526435.1:p.Pro46=
XM_017026989.1:c.708G>C	XP_016882478.1:p.Pro236=
XM_017026990.1:c.705+1607G>C	XP_016882479.1:n.705+1607G>C
NM_030662.4:c.708G>C MANE Select	NP_109587.1:p.Pro236=