Canonical Allele Identifier: CA2661395668

Gene: MBD5

Linked Data

• gnomAD v4: 2-148468342-TGCAACTCCAGTAGTACCTTCTCGGGCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.148468352_148468378del , CM000664.2:g.148468352_148468378del	GRCh38
NC_000002.11:g.149225921_149225947del , CM000664.1:g.149225921_149225947del	GRCh37
NC_000002.10:g.148942391_148942417del	NCBI36
NG_017003.1:g.452342_452368del
NG_017003.2:g.452342_452368del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000638043.2:c.409_435del	ENSP00000490728.2:p.Val137_Pro145del
ENST00000642680.2:c.409_435del MANE Select	ENSP00000493871.2:p.Val137_Pro145del
ENST00000404807.5:c.409_435del	ENSP00000384672.1:p.Val137_Pro145del
ENST00000407073.5:c.409_435del	ENSP00000386049.1:p.Val137_Pro145del
ENST00000627651.2:c.409_435del	ENSP00000486370.1:p.Val137_Pro145del
ENST00000629878.2:c.409_435del	ENSP00000487089.1:p.Val137_Pro145del
NM_018328.4:c.409_435del	NP_060798.2:p.Val137_Pro145del
XM_005263711.2:c.409_435del	XP_005263768.1:p.Val137_Pro145del
XM_011511470.1:c.409_435del	XP_011509772.1:p.Val137_Pro145del
XM_011511471.1:c.409_435del	XP_011509773.1:p.Val137_Pro145del
XM_011511472.1:c.409_435del	XP_011509774.1:p.Val137_Pro145del
XM_011511473.1:c.409_435del	XP_011509775.1:p.Val137_Pro145del
XM_011511474.1:c.409_435del	XP_011509776.1:p.Val137_Pro145del
XM_011511475.1:c.409_435del	XP_011509777.1:p.Val137_Pro145del
XM_011511476.1:c.409_435del	XP_011509778.1:p.Val137_Pro145del
XR_922967.1:n.1638_1664del
XM_011511470.2:c.409_435del	XP_011509772.1:p.Val137_Pro145del
XM_011511472.2:c.409_435del	XP_011509774.1:p.Val137_Pro145del
XM_024452987.1:c.409_435del	XP_024308755.1:p.Val137_Pro145del
XM_024452988.1:c.409_435del	XP_024308756.1:p.Val137_Pro145del
XM_024452989.1:c.409_435del	XP_024308757.1:p.Val137_Pro145del
XM_024452990.1:c.409_435del	XP_024308758.1:p.Val137_Pro145del
XR_002959318.1:n.721_747del
XR_002959319.1:n.721_747del
NM_001378120.1:c.409_435del MANE Select	NP_001365049.1:p.Val137_Pro145del
NM_018328.5:c.409_435del	NP_060798.2:p.Val137_Pro145del