Canonical Allele Identifier: CA2813356119

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4090521G>C , CM000681.2:g.4090521G>C	GRCh38
NC_000019.9:g.4090519G>C , CM000681.1:g.4090519G>C	GRCh37
NC_000019.8:g.4041519G>C	NCBI36
NG_007996.1:g.38608C>G , LRG_750:g.38608C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1719C>G
ENST00000688002.1:n.3431C>G
ENST00000688751.1:n.416C>G
ENST00000689792.1:n.1184C>G
ENST00000262948.10:c.*77C>G MANE Select	ENSP00000262948.4:n.*77C>G
ENST00000262948.9:c.*77C>G	ENSP00000262948.3:n.*77C>G
ENST00000394867.8:c.*77C>G	ENSP00000378336.1:n.*77C>G
ENST00000597263.5:n.465C>G
ENST00000600584.5:n.2729C>G
ENST00000601786.5:n.1581C>G
NM_030662.3:c.*77C>G , LRG_750t1:c.*77C>G	NP_109587.1:n.*77C>G
XM_006722799.2:c.*77C>G	XP_006722862.1:n.*77C>G
XM_011528133.1:c.*77C>G	XP_011526435.1:n.*77C>G
NM_030662.4:c.*77C>G MANE Select	NP_109587.1:n.*77C>G