Canonical Allele Identifier: CA232396

Gene: TDRD5

Linked Data

• ClinVar Variation Id: 92035
• ClinVar RCV Id: RCV000122592
• dbSNP Id: rs386352369
• MyVariant Identifiers: chr1:g.179562889T>C (hg19) ; chr1:g.179593754T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179593754T>C , CM000663.2:g.179593754T>C	GRCh38
NC_000001.10:g.179562889T>C , CM000663.1:g.179562889T>C	GRCh37
NC_000001.9:g.177829512T>C	NCBI36
NG_053092.1:g.7142T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000444136.6:c.527T>C MANE Select	ENSP00000406052.1:p.Phe176Ser
ENST00000294848.12:c.527T>C	ENSP00000294848.8:p.Phe176Ser
ENST00000367614.5:c.527T>C	ENSP00000356586.1:p.Phe176Ser
ENST00000444136.5:c.527T>C	ENSP00000406052.1:p.Phe176Ser
NM_001199085.1:c.527T>C	NP_001186014.1:p.Phe176Ser
NM_001199089.1:c.527T>C	NP_001186018.1:p.Phe176Ser
NM_001199091.1:c.527T>C	NP_001186020.1:p.Phe176Ser
NM_173533.3:c.527T>C	NP_775804.2:p.Phe176Ser
XM_005244934.1:c.527T>C	XP_005244991.1:p.Phe176Ser
XM_005244935.3:c.527T>C	XP_005244992.1:p.Phe176Ser
NM_001199085.2:c.527T>C	NP_001186014.1:p.Phe176Ser
NM_001199089.2:c.527T>C	NP_001186018.1:p.Phe176Ser
NM_001349923.1:c.527T>C	NP_001336852.1:p.Phe176Ser
NM_173533.4:c.527T>C	NP_775804.2:p.Phe176Ser
XM_005244935.4:c.527T>C	XP_005244992.1:p.Phe176Ser
NM_001199085.3:c.527T>C MANE Select	NP_001186014.1:p.Phe176Ser
NM_001199089.3:c.527T>C	NP_001186018.1:p.Phe176Ser
NM_173533.5:c.527T>C	NP_775804.2:p.Phe176Ser
NM_001199091.2:c.527T>C	NP_001186020.1:p.Phe176Ser