Canonical Allele Identifier: CA1296787277

Gene: MBD5

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.148502482A= , CM000664.2:g.148502482A=	GRCh38
NC_000002.11:g.149260051A= , CM000664.1:g.149260051A=	GRCh37
NC_000002.10:g.148976521A=	NCBI36
NG_017003.1:g.486472A=
NG_017003.2:g.486472A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000628572.2:c.2939A=
ENST00000637835.1:n.40A=
ENST00000638043.2:c.4349A=	ENSP00000490728.2:p.Tyr1450=
ENST00000642680.2:c.5009A= MANE Select	ENSP00000493871.2:p.Tyr1670=
ENST00000404807.5:c.5009A=	ENSP00000384672.1:p.Tyr1670=
ENST00000407073.5:c.4310A=	ENSP00000386049.1:p.Tyr1437=
ENST00000416015.2:c.3019A=
ENST00000496893.3:n.2091A=
ENST00000628572.1:c.549A=	ENSP00000486209.1:n.549A=
ENST00000629878.2:c.3216A=	ENSP00000487089.1:p.Leu1072=
ENST00000630352.1:c.162-10388A=
NM_018328.4:c.4310A=	NP_060798.2:p.Tyr1437=
XM_005263711.2:c.5009A=	XP_005263768.1:p.Tyr1670=
XM_011511470.1:c.5048A=	XP_011509772.1:p.Tyr1683=
XM_011511471.1:c.5048A=	XP_011509773.1:p.Tyr1683=
XM_011511472.1:c.5048A=	XP_011509774.1:p.Tyr1683=
XM_011511473.1:c.5048A=	XP_011509775.1:p.Tyr1683=
XM_011511474.1:c.5009A=	XP_011509776.1:p.Tyr1670=
XM_011511475.1:c.4349A=	XP_011509777.1:p.Tyr1450=
XM_011511476.1:c.4310A=	XP_011509778.1:p.Tyr1437=
XR_922967.1:n.6331A=
XM_011511470.2:c.5048A=	XP_011509772.1:p.Tyr1683=
XM_011511472.2:c.5048A=	XP_011509774.1:p.Tyr1683=
XM_024452987.1:c.5009A=	XP_024308755.1:p.Tyr1670=
XM_024452988.1:c.5048A=	XP_024308756.1:p.Tyr1683=
XM_024452989.1:c.5009A=	XP_024308757.1:p.Tyr1670=
XM_024452990.1:c.4349A=	XP_024308758.1:p.Tyr1450=
XR_002959318.1:n.5414A=
XR_002959319.1:n.4815A=
NM_001378120.1:c.5009A= MANE Select	NP_001365049.1:p.Tyr1670=
NM_018328.5:c.4310A=	NP_060798.2:p.Tyr1437=