Canonical Allele Identifier: CA403383369

Gene: MAP2K2

Linked Data

• MyVariant Identifiers: chr19:g.4095420A>T (hg19) ; chr19:g.4095422A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4095422A>T , CM000681.2:g.4095422A>T	GRCh38
NC_000019.9:g.4095420A>T , CM000681.1:g.4095420A>T	GRCh37
NC_000019.8:g.4046420A>T	NCBI36
NG_007996.1:g.33707T>A , LRG_750:g.33707T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1451T>A
ENST00000688002.1:n.3163T>A
ENST00000688751.1:n.148T>A
ENST00000689792.1:n.916T>A
ENST00000262948.10:c.1012T>A MANE Select	ENSP00000262948.4:p.Phe338Ile
ENST00000262948.9:c.1012T>A	ENSP00000262948.3:p.Phe338Ile
ENST00000394867.8:c.721T>A	ENSP00000378336.1:p.Phe241Ile
ENST00000595715.1:n.827T>A
ENST00000597263.5:n.197T>A
ENST00000599021.1:c.122T>A
ENST00000600584.5:n.1572T>A
ENST00000601786.5:n.1313T>A
NM_030662.3:c.1012T>A , LRG_750t1:c.1012T>A	NP_109587.1:p.Phe338Ile
XM_006722799.2:c.733T>A	XP_006722862.1:p.Phe245Ile
XM_011528133.1:c.442T>A	XP_011526435.1:p.Phe148Ile
XM_017026989.1:c.1012T>A	XP_016882478.1:p.Phe338Ile
XM_017026990.1:c.733T>A	XP_016882479.1:p.Phe245Ile
NM_030662.4:c.1012T>A MANE Select	NP_109587.1:p.Phe338Ile