Canonical Allele Identifier: CA2172445061

Gene: MAPKBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41819509G= , CM000677.2:g.41819509G=	GRCh38
NC_000015.9:g.42111707G= , CM000677.1:g.42111707G=	GRCh37
NC_000015.8:g.39898999G=	NCBI36
NG_054745.1:g.50076G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000457542.7:c.2426-86G= MANE Select	ENSP00000397570.2:n.2426-86G=
ENST00000456763.6:c.2444-86G=	ENSP00000393099.2:n.2444-86G=
ENST00000457542.6:c.2426-86G=	ENSP00000397570.2:n.2426-86G=
ENST00000505061.5:n.3003G=
ENST00000505373.5:c.*1977-86G=	ENSP00000421891.1:n.*1977-86G=
ENST00000512970.5:c.*1240-86G=	ENSP00000427582.1:n.*1240-86G=
ENST00000514566.5:c.2426-86G=	ENSP00000426154.1:n.2426-86G=
NM_001128608.1:c.2444-86G=	NP_001122080.1:n.2444-86G=
NM_001265611.1:c.2426-86G=	NP_001252540.1:n.2426-86G=
NM_014994.2:c.2426-86G=	NP_055809.2:n.2426-86G=
NR_049761.1:n.2522-86G=
NR_049762.1:n.2473-86G=
XM_006720438.1:c.2279-86G=	XP_006720501.1:n.2279-86G=
XM_006720439.2:c.695-86G=	XP_006720502.1:n.695-86G=
XM_011521382.1:c.2444-86G=	XP_011519684.1:n.2444-86G=
XM_011521383.1:c.2297-86G=	XP_011519685.1:n.2297-86G=
XM_011521384.1:c.2444-86G=	XP_011519686.1:n.2444-86G=
XM_011521385.1:c.2444-86G=	XP_011519687.1:n.2444-86G=
XM_006720438.2:c.2279-86G=	XP_006720501.1:n.2279-86G=
XM_011521383.2:c.2297-86G=	XP_011519685.1:n.2297-86G=
XM_011521384.3:c.2444-86G=	XP_011519686.1:n.2444-86G=
XM_017022017.1:c.2297-86G=	XP_016877506.1:n.2297-86G=
XR_001751156.2:n.2692-86G=
XR_001751157.2:n.2692-86G=
XR_001751159.2:n.2692-86G=
NM_014994.3:c.2426-86G= MANE Select	NP_055809.2:n.2426-86G=
NM_001128608.2:c.2444-86G=	NP_001122080.1:n.2444-86G=
NM_001265611.2:c.2426-86G=	NP_001252540.1:n.2426-86G=
NR_049761.2:n.2472-86G=
NR_049762.2:n.2423-86G=