Canonical Allele Identifier: CA2184657999

Gene: MAP2K5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67745191G= , CM000677.2:g.67745191G=	GRCh38
NC_000015.9:g.68037529G= , CM000677.1:g.68037529G=	GRCh37
NC_000015.8:g.65824583G=	NCBI36
NG_029143.1:g.207509G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000178640.10:c.1075-3040G= MANE Select	ENSP00000178640.5:n.1075-3040G=
ENST00000178640.9:c.1075-3040G=	ENSP00000178640.5:n.1075-3040G=
ENST00000340972.8:c.505-3040G=	ENSP00000342101.4:n.505-3040G=
ENST00000354498.9:c.967-3040G=	ENSP00000346493.5:n.967-3040G=
ENST00000395476.6:c.1045-3040G=	ENSP00000378859.2:n.1045-3040G=
ENST00000557869.2:c.52-3378G=	ENSP00000483771.1:n.52-3378G=
ENST00000558274.1:n.186-3378G=
ENST00000558392.5:n.901-3040G=
NM_001206804.1:c.967-3040G=	NP_001193733.1:n.967-3040G=
NM_002757.3:c.1045-3040G=	NP_002748.1:n.1045-3040G=
NM_145160.2:c.1075-3040G=	NP_660143.1:n.1075-3040G=
XM_011521784.1:c.1075-3040G=	XP_011520086.1:n.1075-3040G=
XM_011521785.1:c.1075-3040G=	XP_011520087.1:n.1075-3040G=
XM_011521786.1:c.1075-3378G=	XP_011520088.1:n.1075-3378G=
XM_024449988.1:c.844-3040G=	XP_024305756.1:n.844-3040G=
NM_145160.3:c.1075-3040G= MANE Select	NP_660143.1:n.1075-3040G=
NM_001206804.2:c.967-3040G=	NP_001193733.1:n.967-3040G=
NM_002757.4:c.1045-3040G=	NP_002748.1:n.1045-3040G=