Canonical Allele Identifier: CA7302389
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 262515
dbSNP Id: rs114557412

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88839501A>G , CM000676.2:g.88839501A>G GRCh38
NC_000014.8:g.89305845A>G , CM000676.1:g.89305845A>G GRCh37
NC_000014.7:g.88375598A>G NCBI36
NG_008126.1:g.19868A>G
NG_008126.2:g.20349A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380656.7:c.194A>G MANE Select ENSP00000370031.2:p.Asp65Gly
ENST00000338104.10:c.164A>G ENSP00000337653.6:p.Asp55Gly
ENST00000345383.9:c.194A>G ENSP00000339486.6:p.Asp65Gly
ENST00000346301.8:c.164A>G ENSP00000298324.6:p.Asp55Gly
ENST00000354441.10:c.114+14680A>G ENSP00000346427.6:n.114+14680A>G
ENST00000358622.9:c.-399A>G ENSP00000351439.5:n.-399A>G
ENST00000380656.6:c.194A>G ENSP00000370031.2:p.Asp65Gly
ENST00000536576.5:c.164A>G ENSP00000445067.2:p.Asp55Gly
ENST00000554686.5:c.133A>G
ENST00000555057.5:c.164A>G ENSP00000450951.1:p.Asp55Gly
ENST00000556077.5:c.323A>G ENSP00000451034.1:p.Asp108Gly
ENST00000556567.5:n.221A>G
ENST00000556651.5:c.164A>G ENSP00000450993.1:p.Asp55Gly
ENST00000614125.4:c.164A>G ENSP00000482306.1:p.Asp55Gly
ENST00000622513.4:c.164A>G ENSP00000482721.1:p.Asp55Gly
NM_001288781.1:c.164A>G NP_001275710.1:p.Asp55Gly
NM_001288782.1:c.-399A>G NP_001275711.1:n.-399A>G
NM_001288783.1:c.-494A>G NP_001275712.1:n.-494A>G
NM_144596.3:c.194A>G NP_653197.2:p.Asp65Gly
NM_198309.3:c.164A>G NP_938051.1:p.Asp55Gly
NM_198310.3:c.164A>G NP_938052.1:p.Asp55Gly
XM_006720035.1:c.164A>G XP_006720098.1:p.Asp55Gly
XM_006720037.2:c.164A>G XP_006720100.1:p.Asp55Gly
XM_011536432.1:c.164A>G XP_011534734.1:p.Asp55Gly
XM_011536433.1:c.164A>G XP_011534735.1:p.Asp55Gly
XM_011536434.1:c.164A>G XP_011534736.1:p.Asp55Gly
NM_001366535.1:c.164A>G NP_001353464.1:p.Asp55Gly
NM_001366536.1:c.164A>G NP_001353465.1:p.Asp55Gly
NR_159362.1:n.221A>G
XM_011536433.2:c.164A>G XP_011534735.1:p.Asp55Gly
XM_011536434.2:c.164A>G XP_011534736.1:p.Asp55Gly
NM_001366535.2:c.164A>G NP_001353464.1:p.Asp55Gly
NM_001366536.2:c.164A>G NP_001353465.1:p.Asp55Gly
NR_159362.2:n.221A>G
NM_144596.4:c.194A>G MANE Select NP_653197.2:p.Asp65Gly