Canonical Allele Identifier: CA2627947337

Gene: MAPKBP1

Linked Data

• gnomAD v4: 15-41816844-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41816844C>G , CM000677.2:g.41816844C>G	GRCh38
NC_000015.9:g.42109042C>G , CM000677.1:g.42109042C>G	GRCh37
NC_000015.8:g.39896334C>G	NCBI36
NG_054745.1:g.47411C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000457542.7:c.1586-66C>G MANE Select	ENSP00000397570.2:n.1586-66C>G
ENST00000456763.6:c.1604-66C>G	ENSP00000393099.2:n.1604-66C>G
ENST00000457542.6:c.1586-66C>G	ENSP00000397570.2:n.1586-66C>G
ENST00000503526.1:n.373-66C>G
ENST00000505061.5:n.2034-66C>G
ENST00000505373.5:c.*1137-66C>G	ENSP00000421891.1:n.*1137-66C>G
ENST00000512970.5:c.*400-66C>G	ENSP00000427582.1:n.*400-66C>G
ENST00000514566.5:c.1586-66C>G	ENSP00000426154.1:n.1586-66C>G
NM_001128608.1:c.1604-66C>G	NP_001122080.1:n.1604-66C>G
NM_001265611.1:c.1586-66C>G	NP_001252540.1:n.1586-66C>G
NM_014994.2:c.1586-66C>G	NP_055809.2:n.1586-66C>G
NR_049761.1:n.1682-66C>G
NR_049762.1:n.1633-66C>G
XM_006720438.1:c.1439-66C>G	XP_006720501.1:n.1439-66C>G
XM_011521382.1:c.1604-66C>G	XP_011519684.1:n.1604-66C>G
XM_011521383.1:c.1457-66C>G	XP_011519685.1:n.1457-66C>G
XM_011521384.1:c.1604-66C>G	XP_011519686.1:n.1604-66C>G
XM_011521385.1:c.1604-66C>G	XP_011519687.1:n.1604-66C>G
XM_006720438.2:c.1439-66C>G	XP_006720501.1:n.1439-66C>G
XM_011521383.2:c.1457-66C>G	XP_011519685.1:n.1457-66C>G
XM_011521384.3:c.1604-66C>G	XP_011519686.1:n.1604-66C>G
XM_017022017.1:c.1457-66C>G	XP_016877506.1:n.1457-66C>G
XR_001751156.2:n.1852-66C>G
XR_001751157.2:n.1852-66C>G
XR_001751159.2:n.1852-66C>G
NM_014994.3:c.1586-66C>G MANE Select	NP_055809.2:n.1586-66C>G
NM_001128608.2:c.1604-66C>G	NP_001122080.1:n.1604-66C>G
NM_001265611.2:c.1586-66C>G	NP_001252540.1:n.1586-66C>G
NR_049761.2:n.1632-66C>G
NR_049762.2:n.1583-66C>G