Canonical Allele Identifier: CA202465
Gene: TTC8 HGNC NCBI

Linked Data

ClinVar Variation Id: 196600
dbSNP Id: rs150880478

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88840883A>G , CM000676.2:g.88840883A>G GRCh38
NC_000014.8:g.89307227A>G , CM000676.1:g.89307227A>G GRCh37
NC_000014.7:g.88376980A>G NCBI36
NG_008126.1:g.21250A>G
NG_008126.2:g.21731A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000380656.7:c.284A>G MANE Select ENSP00000370031.2:p.Lys95Arg
ENST00000338104.10:c.254A>G ENSP00000337653.6:p.Lys85Arg
ENST00000345383.9:c.284A>G ENSP00000339486.6:p.Lys95Arg
ENST00000346301.8:c.254A>G ENSP00000298324.6:p.Lys85Arg
ENST00000354441.10:c.114+16062A>G ENSP00000346427.6:n.114+16062A>G
ENST00000358622.9:c.-309A>G ENSP00000351439.5:n.-309A>G
ENST00000380656.6:c.284A>G ENSP00000370031.2:p.Lys95Arg
ENST00000536576.5:c.254A>G ENSP00000445067.2:p.Lys85Arg
ENST00000554686.5:c.223A>G
ENST00000555057.5:c.254A>G ENSP00000450951.1:p.Lys85Arg
ENST00000556077.5:c.413A>G ENSP00000451034.1:p.Lys138Arg
ENST00000556133.1:n.45A>G
ENST00000556567.5:n.311A>G
ENST00000556651.5:c.254A>G ENSP00000450993.1:p.Lys85Arg
ENST00000614125.4:c.254A>G ENSP00000482306.1:p.Lys85Arg
ENST00000622513.4:c.254A>G ENSP00000482721.1:p.Lys85Arg
NM_001288781.1:c.254A>G NP_001275710.1:p.Lys85Arg
NM_001288782.1:c.-309A>G NP_001275711.1:n.-309A>G
NM_001288783.1:c.-404A>G NP_001275712.1:n.-404A>G
NM_144596.3:c.284A>G NP_653197.2:p.Lys95Arg
NM_198309.3:c.254A>G NP_938051.1:p.Lys85Arg
NM_198310.3:c.254A>G NP_938052.1:p.Lys85Arg
XM_006720035.1:c.254A>G XP_006720098.1:p.Lys85Arg
XM_006720037.2:c.254A>G XP_006720100.1:p.Lys85Arg
XM_011536432.1:c.254A>G XP_011534734.1:p.Lys85Arg
XM_011536433.1:c.254A>G XP_011534735.1:p.Lys85Arg
XM_011536434.1:c.254A>G XP_011534736.1:p.Lys85Arg
XM_011536435.1:c.-494A>G XP_011534737.1:n.-494A>G
NM_001366535.1:c.254A>G NP_001353464.1:p.Lys85Arg
NM_001366536.1:c.254A>G NP_001353465.1:p.Lys85Arg
NR_159362.1:n.311A>G
XM_011536433.2:c.254A>G XP_011534735.1:p.Lys85Arg
XM_011536434.2:c.254A>G XP_011534736.1:p.Lys85Arg
XM_024449477.1:c.-494A>G XP_024305245.1:n.-494A>G
NM_001366535.2:c.254A>G NP_001353464.1:p.Lys85Arg
NM_001366536.2:c.254A>G NP_001353465.1:p.Lys85Arg
NR_159362.2:n.311A>G
NM_144596.4:c.284A>G MANE Select NP_653197.2:p.Lys95Arg