Canonical Allele Identifier: CA391862788

Gene: MAPKBP1

Linked Data

• MyVariant Identifiers: chr15:g.42109153T>G (hg19) ; chr15:g.41816955T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41816955T>G , CM000677.2:g.41816955T>G	GRCh38
NC_000015.9:g.42109153T>G , CM000677.1:g.42109153T>G	GRCh37
NC_000015.8:g.39896445T>G	NCBI36
NG_054745.1:g.47522T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457542.7:c.1631T>G MANE Select	ENSP00000397570.2:p.Val544Gly
ENST00000456763.6:c.1649T>G	ENSP00000393099.2:p.Val550Gly
ENST00000457542.6:c.1631T>G	ENSP00000397570.2:p.Val544Gly
ENST00000503526.1:n.418T>G
ENST00000505061.5:n.2079T>G
ENST00000505373.5:c.*1182T>G	ENSP00000421891.1:n.*1182T>G
ENST00000512970.5:c.*445T>G	ENSP00000427582.1:n.*445T>G
ENST00000514566.5:c.1631T>G	ENSP00000426154.1:p.Val544Gly
NM_001128608.1:c.1649T>G	NP_001122080.1:p.Val550Gly
NM_001265611.1:c.1631T>G	NP_001252540.1:p.Val544Gly
NM_014994.2:c.1631T>G	NP_055809.2:p.Val544Gly
NR_049761.1:n.1727T>G
NR_049762.1:n.1678T>G
XM_006720438.1:c.1484T>G	XP_006720501.1:p.Val495Gly
XM_006720439.2:c.-97T>G	XP_006720502.1:n.-97T>G
XM_011521382.1:c.1649T>G	XP_011519684.1:p.Val550Gly
XM_011521383.1:c.1502T>G	XP_011519685.1:p.Val501Gly
XM_011521384.1:c.1649T>G	XP_011519686.1:p.Val550Gly
XM_011521385.1:c.1649T>G	XP_011519687.1:p.Val550Gly
XM_006720438.2:c.1484T>G	XP_006720501.1:p.Val495Gly
XM_011521383.2:c.1502T>G	XP_011519685.1:p.Val501Gly
XM_011521384.3:c.1649T>G	XP_011519686.1:p.Val550Gly
XM_017022017.1:c.1502T>G	XP_016877506.1:p.Val501Gly
XR_001751156.2:n.1897T>G
XR_001751157.2:n.1897T>G
XR_001751159.2:n.1897T>G
NM_014994.3:c.1631T>G MANE Select	NP_055809.2:p.Val544Gly
NM_001128608.2:c.1649T>G	NP_001122080.1:p.Val550Gly
NM_001265611.2:c.1631T>G	NP_001252540.1:p.Val544Gly
NR_049761.2:n.1677T>G
NR_049762.2:n.1628T>G