Canonical Allele Identifier: CA348858998

Gene: MBD5

Linked Data

• MyVariant Identifiers: chr2:g.149260020T>A (hg19) ; chr2:g.148502451T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.148502451T>A , CM000664.2:g.148502451T>A	GRCh38
NC_000002.11:g.149260020T>A , CM000664.1:g.149260020T>A	GRCh37
NC_000002.10:g.148976490T>A	NCBI36
NG_017003.1:g.486441T>A
NG_017003.2:g.486441T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000628572.2:c.2908T>A
ENST00000637835.1:n.9T>A
ENST00000638043.2:c.4318T>A	ENSP00000490728.2:p.Leu1440Met
ENST00000642680.2:c.4978T>A MANE Select	ENSP00000493871.2:p.Leu1660Met
ENST00000404807.5:c.4978T>A	ENSP00000384672.1:p.Leu1660Met
ENST00000407073.5:c.4279T>A	ENSP00000386049.1:p.Leu1427Met
ENST00000416015.2:c.2988T>A
ENST00000496893.3:n.2060T>A
ENST00000628572.1:c.518T>A	ENSP00000486209.1:n.518T>A
ENST00000629878.2:c.3185T>A	ENSP00000487089.1:p.Val1062Asp
ENST00000630352.1:c.162-10419T>A
NM_018328.4:c.4279T>A	NP_060798.2:p.Leu1427Met
XM_005263711.2:c.4978T>A	XP_005263768.1:p.Leu1660Met
XM_011511470.1:c.5017T>A	XP_011509772.1:p.Leu1673Met
XM_011511471.1:c.5017T>A	XP_011509773.1:p.Leu1673Met
XM_011511472.1:c.5017T>A	XP_011509774.1:p.Leu1673Met
XM_011511473.1:c.5017T>A	XP_011509775.1:p.Leu1673Met
XM_011511474.1:c.4978T>A	XP_011509776.1:p.Leu1660Met
XM_011511475.1:c.4318T>A	XP_011509777.1:p.Leu1440Met
XM_011511476.1:c.4279T>A	XP_011509778.1:p.Leu1427Met
XR_922967.1:n.6300T>A
XM_011511470.2:c.5017T>A	XP_011509772.1:p.Leu1673Met
XM_011511472.2:c.5017T>A	XP_011509774.1:p.Leu1673Met
XM_024452987.1:c.4978T>A	XP_024308755.1:p.Leu1660Met
XM_024452988.1:c.5017T>A	XP_024308756.1:p.Leu1673Met
XM_024452989.1:c.4978T>A	XP_024308757.1:p.Leu1660Met
XM_024452990.1:c.4318T>A	XP_024308758.1:p.Leu1440Met
XR_002959318.1:n.5383T>A
XR_002959319.1:n.4784T>A
NM_001378120.1:c.4978T>A MANE Select	NP_001365049.1:p.Leu1660Met
NM_018328.5:c.4279T>A	NP_060798.2:p.Leu1427Met