Canonical Allele Identifier: CA536895847
Gene: MBD5 HGNC NCBI

Linked Data

dbSNP Id: rs1236121508

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.148502391T>A , CM000664.2:g.148502391T>A GRCh38
NC_000002.11:g.149259960T>A , CM000664.1:g.149259960T>A GRCh37
NC_000002.10:g.148976430T>A NCBI36
NG_017003.1:g.486381T>A
NG_017003.2:g.486381T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000628572.2:c.2893-45T>A
ENST00000638043.2:c.4264-6T>A ENSP00000490728.2:n.4264-6T>A
ENST00000642680.2:c.4963-45T>A MANE Select ENSP00000493871.2:n.4963-45T>A
ENST00000404807.5:c.4963-45T>A ENSP00000384672.1:n.4963-45T>A
ENST00000407073.5:c.4264-45T>A ENSP00000386049.1:n.4264-45T>A
ENST00000416015.2:c.2973-45T>A
ENST00000496893.3:n.2045-45T>A
ENST00000628572.1:c.503-45T>A ENSP00000486209.1:n.503-45T>A
ENST00000629878.2:c.3170-45T>A ENSP00000487089.1:n.3170-45T>A
ENST00000630352.1:c.162-10479T>A
NM_018328.4:c.4264-45T>A NP_060798.2:n.4264-45T>A
XM_005263711.2:c.4963-45T>A XP_005263768.1:n.4963-45T>A
XM_011511470.1:c.4963-6T>A XP_011509772.1:n.4963-6T>A
XM_011511471.1:c.4963-6T>A XP_011509773.1:n.4963-6T>A
XM_011511472.1:c.4963-6T>A XP_011509774.1:n.4963-6T>A
XM_011511473.1:c.4963-6T>A XP_011509775.1:n.4963-6T>A
XM_011511474.1:c.4963-45T>A XP_011509776.1:n.4963-45T>A
XM_011511475.1:c.4264-6T>A XP_011509777.1:n.4264-6T>A
XM_011511476.1:c.4264-45T>A XP_011509778.1:n.4264-45T>A
XR_922967.1:n.6285-45T>A
XM_011511470.2:c.4963-6T>A XP_011509772.1:n.4963-6T>A
XM_011511472.2:c.4963-6T>A XP_011509774.1:n.4963-6T>A
XM_024452987.1:c.4963-45T>A XP_024308755.1:n.4963-45T>A
XM_024452988.1:c.4963-6T>A XP_024308756.1:n.4963-6T>A
XM_024452989.1:c.4963-45T>A XP_024308757.1:n.4963-45T>A
XM_024452990.1:c.4264-6T>A XP_024308758.1:n.4264-6T>A
XR_002959318.1:n.5368-45T>A
XR_002959319.1:n.4769-45T>A
NM_001378120.1:c.4963-45T>A MANE Select NP_001365049.1:n.4963-45T>A
NM_018328.5:c.4264-45T>A NP_060798.2:n.4264-45T>A