Canonical Allele Identifier: CA2627947367

Gene: MAPKBP1

Linked Data

• gnomAD v4: 15-41816862-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41816862A>T , CM000677.2:g.41816862A>T	GRCh38
NC_000015.9:g.42109060A>T , CM000677.1:g.42109060A>T	GRCh37
NC_000015.8:g.39896352A>T	NCBI36
NG_054745.1:g.47429A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000457542.7:c.1586-48A>T MANE Select	ENSP00000397570.2:n.1586-48A>T
ENST00000456763.6:c.1604-48A>T	ENSP00000393099.2:n.1604-48A>T
ENST00000457542.6:c.1586-48A>T	ENSP00000397570.2:n.1586-48A>T
ENST00000503526.1:n.373-48A>T
ENST00000505061.5:n.2034-48A>T
ENST00000505373.5:c.*1137-48A>T	ENSP00000421891.1:n.*1137-48A>T
ENST00000512970.5:c.*400-48A>T	ENSP00000427582.1:n.*400-48A>T
ENST00000514566.5:c.1586-48A>T	ENSP00000426154.1:n.1586-48A>T
NM_001128608.1:c.1604-48A>T	NP_001122080.1:n.1604-48A>T
NM_001265611.1:c.1586-48A>T	NP_001252540.1:n.1586-48A>T
NM_014994.2:c.1586-48A>T	NP_055809.2:n.1586-48A>T
NR_049761.1:n.1682-48A>T
NR_049762.1:n.1633-48A>T
XM_006720438.1:c.1439-48A>T	XP_006720501.1:n.1439-48A>T
XM_011521382.1:c.1604-48A>T	XP_011519684.1:n.1604-48A>T
XM_011521383.1:c.1457-48A>T	XP_011519685.1:n.1457-48A>T
XM_011521384.1:c.1604-48A>T	XP_011519686.1:n.1604-48A>T
XM_011521385.1:c.1604-48A>T	XP_011519687.1:n.1604-48A>T
XM_006720438.2:c.1439-48A>T	XP_006720501.1:n.1439-48A>T
XM_011521383.2:c.1457-48A>T	XP_011519685.1:n.1457-48A>T
XM_011521384.3:c.1604-48A>T	XP_011519686.1:n.1604-48A>T
XM_017022017.1:c.1457-48A>T	XP_016877506.1:n.1457-48A>T
XR_001751156.2:n.1852-48A>T
XR_001751157.2:n.1852-48A>T
XR_001751159.2:n.1852-48A>T
NM_014994.3:c.1586-48A>T MANE Select	NP_055809.2:n.1586-48A>T
NM_001128608.2:c.1604-48A>T	NP_001122080.1:n.1604-48A>T
NM_001265611.2:c.1586-48A>T	NP_001252540.1:n.1586-48A>T
NR_049761.2:n.1632-48A>T
NR_049762.2:n.1583-48A>T