Canonical Allele Identifier: CA2584876804

Gene: MAP2K2

Linked Data

• gnomAD v4: 19-4094312-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4094312T>C , CM000681.2:g.4094312T>C	GRCh38
NC_000019.9:g.4094310T>C , CM000681.1:g.4094310T>C	GRCh37
NC_000019.8:g.4045310T>C	NCBI36
NG_007996.1:g.34817A>G , LRG_750:g.34817A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1531+141A>G
ENST00000688002.1:n.3243+141A>G
ENST00000688751.1:n.228+141A>G
ENST00000689792.1:n.996+141A>G
ENST00000262948.10:c.1092+141A>G MANE Select	ENSP00000262948.4:n.1092+141A>G
ENST00000262948.9:c.1092+141A>G	ENSP00000262948.3:n.1092+141A>G
ENST00000394867.8:c.801+141A>G	ENSP00000378336.1:n.801+141A>G
ENST00000597263.5:n.277+141A>G
ENST00000599021.1:c.202+141A>G
ENST00000600584.5:n.2541+141A>G
ENST00000601786.5:n.1393+141A>G
NM_030662.3:c.1092+141A>G , LRG_750t1:c.1092+141A>G	NP_109587.1:n.1092+141A>G
XM_006722799.2:c.813+141A>G	XP_006722862.1:n.813+141A>G
XM_011528133.1:c.522+141A>G	XP_011526435.1:n.522+141A>G
NM_030662.4:c.1092+141A>G MANE Select	NP_109587.1:n.1092+141A>G