Canonical Allele Identifier: CA2627948810

Gene: MAPKBP1

Linked Data

• gnomAD v4: 15-41819513-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.41819513G>T , CM000677.2:g.41819513G>T	GRCh38
NC_000015.9:g.42111711G>T , CM000677.1:g.42111711G>T	GRCh37
NC_000015.8:g.39899003G>T	NCBI36
NG_054745.1:g.50080G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000457542.7:c.2426-82G>T MANE Select	ENSP00000397570.2:n.2426-82G>T
ENST00000456763.6:c.2444-82G>T	ENSP00000393099.2:n.2444-82G>T
ENST00000457542.6:c.2426-82G>T	ENSP00000397570.2:n.2426-82G>T
ENST00000505061.5:n.3007G>T
ENST00000505373.5:c.*1977-82G>T	ENSP00000421891.1:n.*1977-82G>T
ENST00000512970.5:c.*1240-82G>T	ENSP00000427582.1:n.*1240-82G>T
ENST00000514566.5:c.2426-82G>T	ENSP00000426154.1:n.2426-82G>T
NM_001128608.1:c.2444-82G>T	NP_001122080.1:n.2444-82G>T
NM_001265611.1:c.2426-82G>T	NP_001252540.1:n.2426-82G>T
NM_014994.2:c.2426-82G>T	NP_055809.2:n.2426-82G>T
NR_049761.1:n.2522-82G>T
NR_049762.1:n.2473-82G>T
XM_006720438.1:c.2279-82G>T	XP_006720501.1:n.2279-82G>T
XM_006720439.2:c.695-82G>T	XP_006720502.1:n.695-82G>T
XM_011521382.1:c.2444-82G>T	XP_011519684.1:n.2444-82G>T
XM_011521383.1:c.2297-82G>T	XP_011519685.1:n.2297-82G>T
XM_011521384.1:c.2444-82G>T	XP_011519686.1:n.2444-82G>T
XM_011521385.1:c.2444-82G>T	XP_011519687.1:n.2444-82G>T
XM_006720438.2:c.2279-82G>T	XP_006720501.1:n.2279-82G>T
XM_011521383.2:c.2297-82G>T	XP_011519685.1:n.2297-82G>T
XM_011521384.3:c.2444-82G>T	XP_011519686.1:n.2444-82G>T
XM_017022017.1:c.2297-82G>T	XP_016877506.1:n.2297-82G>T
XR_001751156.2:n.2692-82G>T
XR_001751157.2:n.2692-82G>T
XR_001751159.2:n.2692-82G>T
NM_014994.3:c.2426-82G>T MANE Select	NP_055809.2:n.2426-82G>T
NM_001128608.2:c.2444-82G>T	NP_001122080.1:n.2444-82G>T
NM_001265611.2:c.2426-82G>T	NP_001252540.1:n.2426-82G>T
NR_049761.2:n.2472-82G>T
NR_049762.2:n.2423-82G>T