Canonical Allele Identifier: CA2584876665

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4090597-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090597G>A , CM000681.2:g.4090597G>A	GRCh38
NC_000019.9:g.4090595G>A , CM000681.1:g.4090595G>A	GRCh37
NC_000019.8:g.4041595G>A	NCBI36
NG_007996.1:g.38532C>T , LRG_750:g.38532C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1643C>T
ENST00000688002.1:n.3355C>T
ENST00000688751.1:n.340C>T
ENST00000689792.1:n.1108C>T
ENST00000262948.10:c.*1C>T MANE Select	ENSP00000262948.4:n.*1C>T
ENST00000262948.9:c.*1C>T	ENSP00000262948.3:n.*1C>T
ENST00000394867.8:c.*1C>T	ENSP00000378336.1:n.*1C>T
ENST00000597263.5:n.389C>T
ENST00000599021.1:c.314C>T
ENST00000600584.5:n.2653C>T
ENST00000601786.5:n.1505C>T
NM_030662.3:c.*1C>T , LRG_750t1:c.*1C>T	NP_109587.1:n.*1C>T
XM_006722799.2:c.*1C>T	XP_006722862.1:n.*1C>T
XM_011528133.1:c.*1C>T	XP_011526435.1:n.*1C>T
NM_030662.4:c.*1C>T MANE Select	NP_109587.1:n.*1C>T