Canonical Allele Identifier: CA2584877158

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094705-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094705G>T , CM000681.2:g.4094705G>T	GRCh38
NC_000019.9:g.4094703G>T , CM000681.1:g.4094703G>T	GRCh37
NC_000019.8:g.4045703G>T	NCBI36
NG_007996.1:g.34424C>A , LRG_750:g.34424C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1486-207C>A
ENST00000688002.1:n.3198-207C>A
ENST00000688751.1:n.183-207C>A
ENST00000689792.1:n.951-207C>A
ENST00000262948.10:c.1047-207C>A MANE Select	ENSP00000262948.4:n.1047-207C>A
ENST00000262948.9:c.1047-207C>A	ENSP00000262948.3:n.1047-207C>A
ENST00000394867.8:c.756-207C>A	ENSP00000378336.1:n.756-207C>A
ENST00000597263.5:n.232-207C>A
ENST00000599021.1:c.157-207C>A
ENST00000600584.5:n.2289C>A
ENST00000601786.5:n.1348-207C>A
NM_030662.3:c.1047-207C>A , LRG_750t1:c.1047-207C>A	NP_109587.1:n.1047-207C>A
XM_006722799.2:c.768-207C>A	XP_006722862.1:n.768-207C>A
XM_011528133.1:c.477-207C>A	XP_011526435.1:n.477-207C>A
XM_017026989.1:c.1388C>A	XP_016882478.1:p.Pro463His
XM_017026990.1:c.1109C>A	XP_016882479.1:p.Pro370His
NM_030662.4:c.1047-207C>A MANE Select	NP_109587.1:n.1047-207C>A