Canonical Allele Identifier: CA2172443942
Gene: MAPKBP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.41816855C= , CM000677.2:g.41816855C= GRCh38
NC_000015.9:g.42109053C= , CM000677.1:g.42109053C= GRCh37
NC_000015.8:g.39896345C= NCBI36
NG_054745.1:g.47422C=

Transcript Alleles

HGVS Amino-acid change
ENST00000457542.7:c.1586-55C= MANE Select ENSP00000397570.2:n.1586-55C=
ENST00000456763.6:c.1604-55C= ENSP00000393099.2:n.1604-55C=
ENST00000457542.6:c.1586-55C= ENSP00000397570.2:n.1586-55C=
ENST00000503526.1:n.373-55C=
ENST00000505061.5:n.2034-55C=
ENST00000505373.5:c.*1137-55C= ENSP00000421891.1:n.*1137-55C=
ENST00000512970.5:c.*400-55C= ENSP00000427582.1:n.*400-55C=
ENST00000514566.5:c.1586-55C= ENSP00000426154.1:n.1586-55C=
NM_001128608.1:c.1604-55C= NP_001122080.1:n.1604-55C=
NM_001265611.1:c.1586-55C= NP_001252540.1:n.1586-55C=
NM_014994.2:c.1586-55C= NP_055809.2:n.1586-55C=
NR_049761.1:n.1682-55C=
NR_049762.1:n.1633-55C=
XM_006720438.1:c.1439-55C= XP_006720501.1:n.1439-55C=
XM_011521382.1:c.1604-55C= XP_011519684.1:n.1604-55C=
XM_011521383.1:c.1457-55C= XP_011519685.1:n.1457-55C=
XM_011521384.1:c.1604-55C= XP_011519686.1:n.1604-55C=
XM_011521385.1:c.1604-55C= XP_011519687.1:n.1604-55C=
XM_006720438.2:c.1439-55C= XP_006720501.1:n.1439-55C=
XM_011521383.2:c.1457-55C= XP_011519685.1:n.1457-55C=
XM_011521384.3:c.1604-55C= XP_011519686.1:n.1604-55C=
XM_017022017.1:c.1457-55C= XP_016877506.1:n.1457-55C=
XR_001751156.2:n.1852-55C=
XR_001751157.2:n.1852-55C=
XR_001751159.2:n.1852-55C=
NM_014994.3:c.1586-55C= MANE Select NP_055809.2:n.1586-55C=
NM_001128608.2:c.1604-55C= NP_001122080.1:n.1604-55C=
NM_001265611.2:c.1586-55C= NP_001252540.1:n.1586-55C=
NR_049761.2:n.1632-55C=
NR_049762.2:n.1583-55C=