Canonical Allele Identifier: CA613565674
Gene: TTC6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.37597370A>T , CM000676.2:g.37597370A>T GRCh38
NC_000014.8:g.38066575A>T , CM000676.1:g.38066575A>T GRCh37
NC_000014.7:g.37136326A>T NCBI36
NG_033028.1:g.2751T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000553443.6:c.-96+1362A>T MANE Select ENSP00000451131.1:n.-96+1362A>T
ENST00000556845.1:c.-235+1362A>T ENSP00000450572.1:n.-235+1362A>T
NM_001310135.1:c.-48+1362A>T NP_001297064.1:n.-48+1362A>T
XM_011537432.1:c.-48+1362A>T XP_011535734.1:n.-48+1362A>T
XR_943762.1:n.810+1362A>T
XM_011537432.2:c.-48+1362A>T XP_011535734.1:n.-48+1362A>T
XM_017021254.1:c.-48+1362A>T XP_016876743.1:n.-48+1362A>T
XM_017021255.1:c.-48+1362A>T XP_016876744.1:n.-48+1362A>T
XM_017021257.1:c.-48+1362A>T XP_016876746.1:n.-48+1362A>T
XM_024449560.1:c.-308+3816A>T XP_024305328.1:n.-308+3816A>T
XR_001750287.1:n.810+1362A>T
XR_943762.2:n.810+1362A>T
NM_001310135.2:c.-48+1362A>T NP_001297064.1:n.-48+1362A>T
NM_001310135.3:c.-48+1362A>T NP_001297064.1:n.-48+1362A>T
NM_001310135.5:c.-96+1362A>T MANE Select NP_001297064.2:n.-96+1362A>T
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