Canonical Allele Identifier: CA403383465

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4095446-G-A
• MyVariant Identifiers: chr19:g.4095444G>A (hg19) ; chr19:g.4095446G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095446G>A , CM000681.2:g.4095446G>A	GRCh38
NC_000019.9:g.4095444G>A , CM000681.1:g.4095444G>A	GRCh37
NC_000019.8:g.4046444G>A	NCBI36
NG_007996.1:g.33683C>T , LRG_750:g.33683C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1427C>T
ENST00000688002.1:n.3139C>T
ENST00000688751.1:n.124C>T
ENST00000689792.1:n.892C>T
ENST00000262948.10:c.988C>T MANE Select	ENSP00000262948.4:p.Pro330Ser
ENST00000262948.9:c.988C>T	ENSP00000262948.3:p.Pro330Ser
ENST00000394867.8:c.697C>T	ENSP00000378336.1:p.Pro233Ser
ENST00000595715.1:n.803C>T
ENST00000597263.5:n.173C>T
ENST00000599021.1:c.98C>T
ENST00000600584.5:n.1548C>T
ENST00000601786.5:n.1289C>T
NM_030662.3:c.988C>T , LRG_750t1:c.988C>T	NP_109587.1:p.Pro330Ser
XM_006722799.2:c.709C>T	XP_006722862.1:p.Pro237Ser
XM_011528133.1:c.418C>T	XP_011526435.1:p.Pro140Ser
XM_017026989.1:c.988C>T	XP_016882478.1:p.Pro330Ser
XM_017026990.1:c.709C>T	XP_016882479.1:p.Pro237Ser
NM_030662.4:c.988C>T MANE Select	NP_109587.1:p.Pro330Ser