Canonical Allele Identifier: CA2658921473
Gene: TTC7A HGNC NCBI

Linked Data

gnomAD v4: 2-46950291-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.46950291A>G , CM000664.2:g.46950291A>G GRCh38
NC_000002.11:g.47177430A>G , CM000664.1:g.47177430A>G GRCh37
NC_000002.10:g.47030934A>G NCBI36
NG_034143.1:g.39163A>G
NG_034143.2:g.39163A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698500.1:n.804-72A>G
ENST00000698501.1:n.506-72A>G
ENST00000698502.1:n.166-72A>G
ENST00000319190.11:c.185-72A>G MANE Select ENSP00000316699.5:n.185-72A>G
ENST00000319190.9:c.185-72A>G ENSP00000316699.5:n.185-72A>G
ENST00000394850.6:c.185-72A>G ENSP00000378320.2:n.185-72A>G
ENST00000409245.5:c.83-72A>G ENSP00000386307.1:n.83-72A>G
ENST00000441914.5:c.184-72A>G
ENST00000461601.5:n.452-72A>G
NM_001288951.1:c.185-72A>G NP_001275880.1:n.185-72A>G
NM_001288953.1:c.83-72A>G NP_001275882.1:n.83-72A>G
NM_001288955.1:c.-720-72A>G NP_001275884.1:n.-720-72A>G
NM_020458.3:c.185-72A>G NP_065191.2:n.185-72A>G
XM_011532999.1:c.185-72A>G XP_011531301.1:n.185-72A>G
XR_939696.1:n.490-72A>G
XM_005264439.4:c.-231-72A>G XP_005264496.1:n.-231-72A>G
XM_011532998.3:c.-296-72A>G XP_011531300.1:n.-296-72A>G
XM_011532999.2:c.185-72A>G XP_011531301.1:n.185-72A>G
XM_017004524.1:c.185-72A>G XP_016860013.1:n.185-72A>G
XM_017004525.1:c.17-72A>G XP_016860014.1:n.17-72A>G
XM_017004526.1:c.185-72A>G XP_016860015.1:n.185-72A>G
XM_017004529.1:c.185-72A>G XP_016860018.1:n.185-72A>G
XR_001738853.2:n.497-72A>G
XR_001738854.1:n.496-72A>G
NM_020458.4:c.185-72A>G MANE Select NP_065191.2:n.185-72A>G
NM_001288951.2:c.185-72A>G NP_001275880.1:n.185-72A>G
NM_001288953.2:c.83-72A>G NP_001275882.1:n.83-72A>G
NM_001288955.2:c.-720-72A>G NP_001275884.1:n.-720-72A>G