Canonical Allele Identifier: CA391862731

Gene: MAPKBP1

Linked Data

• MyVariant Identifiers: chr15:g.42109139C>G (hg19) ; chr15:g.41816941C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41816941C>G , CM000677.2:g.41816941C>G	GRCh38
NC_000015.9:g.42109139C>G , CM000677.1:g.42109139C>G	GRCh37
NC_000015.8:g.39896431C>G	NCBI36
NG_054745.1:g.47508C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457542.7:c.1617C>G MANE Select	ENSP00000397570.2:p.Asp539Glu
ENST00000456763.6:c.1635C>G	ENSP00000393099.2:p.Asp545Glu
ENST00000457542.6:c.1617C>G	ENSP00000397570.2:p.Asp539Glu
ENST00000503526.1:n.404C>G
ENST00000505061.5:n.2065C>G
ENST00000505373.5:c.*1168C>G	ENSP00000421891.1:n.*1168C>G
ENST00000512970.5:c.*431C>G	ENSP00000427582.1:n.*431C>G
ENST00000514566.5:c.1617C>G	ENSP00000426154.1:p.Asp539Glu
NM_001128608.1:c.1635C>G	NP_001122080.1:p.Asp545Glu
NM_001265611.1:c.1617C>G	NP_001252540.1:p.Asp539Glu
NM_014994.2:c.1617C>G	NP_055809.2:p.Asp539Glu
NR_049761.1:n.1713C>G
NR_049762.1:n.1664C>G
XM_006720438.1:c.1470C>G	XP_006720501.1:p.Asp490Glu
XM_011521382.1:c.1635C>G	XP_011519684.1:p.Asp545Glu
XM_011521383.1:c.1488C>G	XP_011519685.1:p.Asp496Glu
XM_011521384.1:c.1635C>G	XP_011519686.1:p.Asp545Glu
XM_011521385.1:c.1635C>G	XP_011519687.1:p.Asp545Glu
XM_006720438.2:c.1470C>G	XP_006720501.1:p.Asp490Glu
XM_011521383.2:c.1488C>G	XP_011519685.1:p.Asp496Glu
XM_011521384.3:c.1635C>G	XP_011519686.1:p.Asp545Glu
XM_017022017.1:c.1488C>G	XP_016877506.1:p.Asp496Glu
XR_001751156.2:n.1883C>G
XR_001751157.2:n.1883C>G
XR_001751159.2:n.1883C>G
NM_014994.3:c.1617C>G MANE Select	NP_055809.2:p.Asp539Glu
NM_001128608.2:c.1635C>G	NP_001122080.1:p.Asp545Glu
NM_001265611.2:c.1617C>G	NP_001252540.1:p.Asp539Glu
NR_049761.2:n.1663C>G
NR_049762.2:n.1614C>G