Canonical Allele Identifier: CA391862638

Gene: MAPKBP1

Linked Data

• MyVariant Identifiers: chr15:g.42109131A>C (hg19) ; chr15:g.41816933A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41816933A>C , CM000677.2:g.41816933A>C	GRCh38
NC_000015.9:g.42109131A>C , CM000677.1:g.42109131A>C	GRCh37
NC_000015.8:g.39896423A>C	NCBI36
NG_054745.1:g.47500A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000457542.7:c.1609A>C MANE Select	ENSP00000397570.2:p.Ser537Arg
ENST00000456763.6:c.1627A>C	ENSP00000393099.2:p.Ser543Arg
ENST00000457542.6:c.1609A>C	ENSP00000397570.2:p.Ser537Arg
ENST00000503526.1:n.396A>C
ENST00000505061.5:n.2057A>C
ENST00000505373.5:c.*1160A>C	ENSP00000421891.1:n.*1160A>C
ENST00000512970.5:c.*423A>C	ENSP00000427582.1:n.*423A>C
ENST00000514566.5:c.1609A>C	ENSP00000426154.1:p.Ser537Arg
NM_001128608.1:c.1627A>C	NP_001122080.1:p.Ser543Arg
NM_001265611.1:c.1609A>C	NP_001252540.1:p.Ser537Arg
NM_014994.2:c.1609A>C	NP_055809.2:p.Ser537Arg
NR_049761.1:n.1705A>C
NR_049762.1:n.1656A>C
XM_006720438.1:c.1462A>C	XP_006720501.1:p.Ser488Arg
XM_011521382.1:c.1627A>C	XP_011519684.1:p.Ser543Arg
XM_011521383.1:c.1480A>C	XP_011519685.1:p.Ser494Arg
XM_011521384.1:c.1627A>C	XP_011519686.1:p.Ser543Arg
XM_011521385.1:c.1627A>C	XP_011519687.1:p.Ser543Arg
XM_006720438.2:c.1462A>C	XP_006720501.1:p.Ser488Arg
XM_011521383.2:c.1480A>C	XP_011519685.1:p.Ser494Arg
XM_011521384.3:c.1627A>C	XP_011519686.1:p.Ser543Arg
XM_017022017.1:c.1480A>C	XP_016877506.1:p.Ser494Arg
XR_001751156.2:n.1875A>C
XR_001751157.2:n.1875A>C
XR_001751159.2:n.1875A>C
NM_014994.3:c.1609A>C MANE Select	NP_055809.2:p.Ser537Arg
NM_001128608.2:c.1627A>C	NP_001122080.1:p.Ser543Arg
NM_001265611.2:c.1609A>C	NP_001252540.1:p.Ser537Arg
NR_049761.2:n.1655A>C
NR_049762.2:n.1606A>C