Canonical Allele Identifier: CA2172442134

Gene: MAPKBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41812609C= , CM000677.2:g.41812609C=	GRCh38
NC_000015.9:g.42104807C= , CM000677.1:g.42104807C=	GRCh37
NC_000015.8:g.39892099C=	NCBI36
NG_054745.1:g.43176C=

Transcript Alleles

HGVS	Amino-acid Change
NM_014994.3:c.592C= MANE Select	NP_055809.2:p.Arg198=
ENST00000457542.7:c.592C= MANE Select	ENSP00000397570.2:p.Arg198=
NM_001128608.1:c.592C=	NP_001122080.1:p.Arg198=
NM_001128608.2:c.592C=	NP_001122080.1:p.Arg198=
NM_001265611.1:c.592C=	NP_001252540.1:p.Arg198=
NM_001265611.2:c.592C=	NP_001252540.1:p.Arg198=
NM_014994.2:c.592C=	NP_055809.2:p.Arg198=
NR_049761.1:n.878C=
NR_049761.2:n.828C=
NR_049762.1:n.786C=
NR_049762.2:n.736C=
ENST00000456763.6:c.592C=	ENSP00000393099.2:p.Arg198=
ENST00000457542.6:c.592C=	ENSP00000397570.2:p.Arg198=
ENST00000502292.5:n.764C=
ENST00000505061.5:n.557C=
ENST00000505373.5:c.*290C=	ENSP00000421891.1:n.*290C=
ENST00000512970.5:c.592C=	ENSP00000427582.1:p.Arg198=
ENST00000514566.5:c.592C=	ENSP00000426154.1:p.Arg198=
ENST00000515164.1:n.577C=
XM_006720438.1:c.592C=	XP_006720501.1:p.Arg198=
XM_006720438.2:c.592C=	XP_006720501.1:p.Arg198=
XM_011521382.1:c.592C=	XP_011519684.1:p.Arg198=
XM_011521383.1:c.592C=	XP_011519685.1:p.Arg198=
XM_011521383.2:c.592C=	XP_011519685.1:p.Arg198=
XM_011521384.1:c.592C=	XP_011519686.1:p.Arg198=
XM_011521384.3:c.592C=	XP_011519686.1:p.Arg198=
XM_011521385.1:c.592C=	XP_011519687.1:p.Arg198=
XM_017022017.1:c.592C=	XP_016877506.1:p.Arg198=
XR_001751156.2:n.840C=
XR_001751157.2:n.840C=
XR_001751159.2:n.840C=