Canonical Allele Identifier: CA354467608

Gene: IFT122 MBD4

Linked Data

• ClinVar Variation Id: 2832220
• ClinVar RCV Id: RCV003689397
• dbSNP Id: rs1375736849
• gnomAD v3: 3-129437015-G-T
• gnomAD v4: 3-129437015-G-T
• MyVariant Identifiers: chr3:g.129155858G>T (hg19) ; chr3:g.129437015G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.129437015G>T , CM000665.2:g.129437015G>T	GRCh38
NC_000003.11:g.129155858G>T , CM000665.1:g.129155858G>T	GRCh37
NC_000003.10:g.130638548G>T	NCBI36
NG_023392.1:g.1891G>T
NG_033106.1:g.8165C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687461.1:n.288+3783G>T (IFT122)
ENST00000693654.1:n.355+3783G>T (IFT122)
ENST00000429544.7:c.629C>A (MBD4) MANE Select	ENSP00000394080.2:p.Thr210Asn
ENST00000249910.5:c.629C>A (MBD4)	ENSP00000249910.1:p.Thr210Asn
ENST00000393278.6:c.247+793C>A (MBD4)	ENSP00000376959.2:n.247+793C>A
ENST00000429544.6:c.629C>A (MBD4)	ENSP00000394080.2:p.Thr210Asn
ENST00000503197.5:c.629C>A (MBD4)	ENSP00000424873.1:p.Thr210Asn
ENST00000507208.1:c.629C>A (MBD4)	ENSP00000422327.1:p.Thr210Asn
ENST00000509587.1:n.442+705C>A (MBD4)
ENST00000509828.1:c.104+2715C>A (MBD4)	ENSP00000422690.1:n.104+2715C>A
NM_001276270.1:c.629C>A (MBD4)	NP_001263199.1:p.Thr210Asn
NM_001276271.1:c.629C>A (MBD4)	NP_001263200.1:p.Thr210Asn
NM_001276272.1:c.629C>A (MBD4)	NP_001263201.1:p.Thr210Asn
NM_001276273.1:c.247+793C>A (MBD4)	NP_001263202.1:n.247+793C>A
NM_003925.2:c.629C>A (MBD4)	NP_003916.1:p.Thr210Asn
XM_011513267.1:c.629C>A (MBD4)	XP_011511569.1:p.Thr210Asn
XM_011513268.1:c.16+705C>A (MBD4)	XP_011511570.1:n.16+705C>A
XM_024453810.1:c.629C>A (MBD4)	XP_024309578.1:p.Thr210Asn
NM_001276270.2:c.629C>A (MBD4) MANE Select	NP_001263199.1:p.Thr210Asn
NM_001276272.2:c.629C>A (MBD4)	NP_001263201.1:p.Thr210Asn
NM_003925.3:c.629C>A (MBD4)	NP_003916.1:p.Thr210Asn
NM_001276271.2:c.629C>A (MBD4)	NP_001263200.1:p.Thr210Asn
NM_001276273.2:c.247+793C>A (MBD4)	NP_001263202.1:n.247+793C>A