Canonical Allele Identifier: CA2319224276

Gene: MAP2K2

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.4099080A= , CM000681.2:g.4099080A=	GRCh38
NC_000019.9:g.4099078A= , CM000681.1:g.4099078A=	GRCh37
NC_000019.8:g.4050078A=	NCBI36
NG_007996.1:g.30049T= , LRG_750:g.30049T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394867.9:n.1358+121T=
ENST00000687128.1:n.1479T=
ENST00000688002.1:n.1334T=
ENST00000689792.1:n.823+121T=
ENST00000262948.10:c.919+121T= MANE Select	ENSP00000262948.4:n.919+121T=
ENST00000262948.9:c.919+121T=	ENSP00000262948.3:n.919+121T=
ENST00000394867.8:c.628+121T=	ENSP00000378336.1:n.628+121T=
ENST00000595715.1:n.734+121T=
ENST00000597263.5:n.169+1939T=
ENST00000599021.1:c.30-1737T=
ENST00000600584.5:n.1479+121T=
ENST00000601786.5:n.1220+121T=
NM_030662.3:c.919+121T= , LRG_750t1:c.919+121T=	NP_109587.1:n.919+121T=
XM_006722799.2:c.705+1939T=	XP_006722862.1:n.705+1939T=
XM_011528133.1:c.349+121T=	XP_011526435.1:n.349+121T=
XM_017026989.1:c.919+121T=	XP_016882478.1:n.919+121T=
XM_017026990.1:c.705+1939T=	XP_016882479.1:n.705+1939T=
NM_030662.4:c.919+121T= MANE Select	NP_109587.1:n.919+121T=