Canonical Allele Identifier: CA2184665034

Gene: MAP2K5

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.67762050G= , CM000677.2:g.67762050G=	GRCh38
NC_000015.9:g.68054388G= , CM000677.1:g.68054388G=	GRCh37
NC_000015.8:g.65841442G=	NCBI36
NG_029143.1:g.224368G=

Transcript Alleles

HGVS	Amino-acid Change
NM_145160.3:c.1135-7552G= MANE Select	NP_660143.1:n.1135-7552G=
ENST00000178640.10:c.1135-7552G= MANE Select	ENSP00000178640.5:n.1135-7552G=
NM_001206804.1:c.1027-7552G=	NP_001193733.1:n.1027-7552G=
NM_001206804.2:c.1027-7552G=	NP_001193733.1:n.1027-7552G=
NM_002757.3:c.1105-7552G=	NP_002748.1:n.1105-7552G=
NM_002757.4:c.1105-7552G=	NP_002748.1:n.1105-7552G=
NM_145160.2:c.1135-7552G=	NP_660143.1:n.1135-7552G=
ENST00000178640.9:c.1135-7552G=	ENSP00000178640.5:n.1135-7552G=
ENST00000340972.8:c.565-7552G=	ENSP00000342101.4:n.565-7552G=
ENST00000354498.9:c.1027-7552G=	ENSP00000346493.5:n.1027-7552G=
ENST00000395476.6:c.1105-7552G=	ENSP00000378859.2:n.1105-7552G=
ENST00000557869.2:c.85-7552G=	ENSP00000483771.1:n.85-7552G=
ENST00000558021.1:n.235-7552G=
ENST00000558274.1:n.219-7552G=
ENST00000558392.5:n.961-7552G=
XM_011521784.1:c.1135-4672G=	XP_011520086.1:n.1135-4672G=
XM_011521785.1:c.1135-4672G=	XP_011520087.1:n.1135-4672G=
XM_011521786.1:c.1108-7552G=	XP_011520088.1:n.1108-7552G=
XM_024449988.1:c.904-7552G=	XP_024305756.1:n.904-7552G=