Canonical Allele Identifier: CA2584876632

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4090552-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090552G>T , CM000681.2:g.4090552G>T	GRCh38
NC_000019.9:g.4090550G>T , CM000681.1:g.4090550G>T	GRCh37
NC_000019.8:g.4041550G>T	NCBI36
NG_007996.1:g.38577C>A , LRG_750:g.38577C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1688C>A
ENST00000688002.1:n.3400C>A
ENST00000688751.1:n.385C>A
ENST00000689792.1:n.1153C>A
ENST00000262948.10:c.*46C>A MANE Select	ENSP00000262948.4:n.*46C>A
ENST00000262948.9:c.*46C>A	ENSP00000262948.3:n.*46C>A
ENST00000394867.8:c.*46C>A	ENSP00000378336.1:n.*46C>A
ENST00000597263.5:n.434C>A
ENST00000600584.5:n.2698C>A
ENST00000601786.5:n.1550C>A
NM_030662.3:c.*46C>A , LRG_750t1:c.*46C>A	NP_109587.1:n.*46C>A
XM_006722799.2:c.*46C>A	XP_006722862.1:n.*46C>A
XM_011528133.1:c.*46C>A	XP_011526435.1:n.*46C>A
NM_030662.4:c.*46C>A MANE Select	NP_109587.1:n.*46C>A