Canonical Allele Identifier: CA769402841
Gene: TTC7A HGNC NCBI

Linked Data

dbSNP Id: rs1416001964

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47002970_47002971insACAAAAC , CM000664.2:g.47002970_47002971insACAAAAC GRCh38
NC_000002.11:g.47230109_47230110insACAAAAC , CM000664.1:g.47230109_47230110insACAAAAC GRCh37
NC_000002.10:g.47083613_47083614insACAAAAC NCBI36
NG_034143.1:g.91842_91843insACAAAAC
NG_034143.2:g.91842_91843insACAAAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000698500.1:n.2899-2952_2899-2951insACAAAAC
ENST00000319190.11:c.1066-2952_1066-2951insACAAAAC MANE Select ENSP00000316699.5:n.1066-2952_1066-2951insACAAAAC
ENST00000319190.9:c.1066-2952_1066-2951insACAAAAC ENSP00000316699.5:n.1066-2952_1066-2951insACAAAAC
ENST00000394850.6:c.1066-2952_1066-2951insACAAAAC ENSP00000378320.2:n.1066-2952_1066-2951insACAAAAC
ENST00000409245.5:c.964-2952_964-2951insACAAAAC ENSP00000386307.1:n.964-2952_964-2951insACAAAAC
ENST00000409825.5:c.1014-2952_1014-2951insACAAAAC
ENST00000441914.5:c.907-2952_907-2951insACAAAAC
ENST00000461601.5:n.1391-2952_1391-2951insACAAAAC
ENST00000474321.6:n.550-2952_550-2951insACAAAAC
ENST00000484061.5:n.349-2952_349-2951insACAAAAC
ENST00000491786.5:n.470-2952_470-2951insACAAAAC
NM_001288951.1:c.1066-2952_1066-2951insACAAAAC NP_001275880.1:n.1066-2952_1066-2951insACAAAAC
NM_001288953.1:c.964-2952_964-2951insACAAAAC NP_001275882.1:n.964-2952_964-2951insACAAAAC
NM_001288955.1:c.4-2952_4-2951insACAAAAC NP_001275884.1:n.4-2952_4-2951insACAAAAC
NM_020458.3:c.1066-2952_1066-2951insACAAAAC NP_065191.2:n.1066-2952_1066-2951insACAAAAC
XM_005264439.2:c.709-2952_709-2951insACAAAAC XP_005264496.1:n.709-2952_709-2951insACAAAAC
XM_011532998.1:c.709-2952_709-2951insACAAAAC XP_011531300.1:n.709-2952_709-2951insACAAAAC
XM_011532999.1:c.1066-2952_1066-2951insACAAAAC XP_011531301.1:n.1066-2952_1066-2951insACAAAAC
XM_011533000.1:c.286-2952_286-2951insACAAAAC XP_011531302.1:n.286-2952_286-2951insACAAAAC
XR_939696.1:n.1371-2952_1371-2951insACAAAAC
XM_005264439.4:c.709-2952_709-2951insACAAAAC XP_005264496.1:n.709-2952_709-2951insACAAAAC
XM_011532998.3:c.709-2952_709-2951insACAAAAC XP_011531300.1:n.709-2952_709-2951insACAAAAC
XM_011532999.2:c.1066-2952_1066-2951insACAAAAC XP_011531301.1:n.1066-2952_1066-2951insACAAAAC
XM_011533000.3:c.286-2952_286-2951insACAAAAC XP_011531302.1:n.286-2952_286-2951insACAAAAC
XM_017004524.1:c.1066-2952_1066-2951insACAAAAC XP_016860013.1:n.1066-2952_1066-2951insACAAAAC
XM_017004525.1:c.898-2952_898-2951insACAAAAC XP_016860014.1:n.898-2952_898-2951insACAAAAC
XM_017004526.1:c.1066-2952_1066-2951insACAAAAC XP_016860015.1:n.1066-2952_1066-2951insACAAAAC
XM_017004529.1:c.1066-2952_1066-2951insACAAAAC XP_016860018.1:n.1066-2952_1066-2951insACAAAAC
XM_024453013.1:c.31-2952_31-2951insACAAAAC XP_024308781.1:n.31-2952_31-2951insACAAAAC
XR_001738853.2:n.1378-2952_1378-2951insACAAAAC
XR_001738854.1:n.1377-2952_1377-2951insACAAAAC
NM_020458.4:c.1066-2952_1066-2951insACAAAAC MANE Select NP_065191.2:n.1066-2952_1066-2951insACAAAAC
NM_001288951.2:c.1066-2952_1066-2951insACAAAAC NP_001275880.1:n.1066-2952_1066-2951insACAAAAC
NM_001288953.2:c.964-2952_964-2951insACAAAAC NP_001275882.1:n.964-2952_964-2951insACAAAAC
NM_001288955.2:c.4-2952_4-2951insACAAAAC NP_001275884.1:n.4-2952_4-2951insACAAAAC