Canonical Allele Identifier: CA346717512

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47073732A>T , CM000664.2:g.47073732A>T GRCh38
NC_000002.11:g.47300871A>T , CM000664.1:g.47300871A>T GRCh37
NC_000002.10:g.47154375A>T NCBI36
NG_034143.1:g.162604A>T
NG_034143.2:g.162604A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698500.1:n.4219A>T (TTC7A)
ENST00000698503.1:n.2392A>T (TTC7A)
ENST00000698504.1:n.467A>T (TTC7A)
ENST00000319190.11:c.2386A>T (TTC7A) MANE Select ENSP00000316699.5:p.Ser796Cys
ENST00000651101.1:n.984A>T (TTC7A)
ENST00000651415.1:n.1177A>T (TTC7A)
ENST00000652236.1:n.1087A>T (TTC7A)
ENST00000652568.1:n.1059A>T (TTC7A)
ENST00000319190.9:c.2386A>T (TTC7A) ENSP00000316699.5:p.Ser796Cys
ENST00000394850.6:c.2458A>T (TTC7A) ENSP00000378320.2:p.Ser820Cys
ENST00000409245.5:c.2284A>T (TTC7A) ENSP00000386307.1:p.Ser762Cys
ENST00000409825.5:c.2334A>T (TTC7A)
ENST00000422269.1:c.787-7595T>A
ENST00000441914.5:c.2227A>T (TTC7A)
ENST00000464527.2:n.399-7595T>A (STPG4)
ENST00000482548.1:n.402-5176T>A (STPG4)
ENST00000484061.5:n.1493A>T (TTC7A)
ENST00000491786.5:n.1790A>T (TTC7A)
ENST00000496939.1:n.416-26813T>A (STPG4)
NM_001288951.1:c.2458A>T (TTC7A) NP_001275880.1:p.Ser820Cys
NM_001288953.1:c.2284A>T (TTC7A) NP_001275882.1:p.Ser762Cys
NM_001288955.1:c.1324A>T (TTC7A) NP_001275884.1:p.Ser442Cys
NM_020458.3:c.2386A>T (TTC7A) NP_065191.2:p.Ser796Cys
XM_005264439.2:c.2029A>T (TTC7A) XP_005264496.1:p.Ser677Cys
XM_011532998.1:c.2029A>T (TTC7A) XP_011531300.1:p.Ser677Cys
XM_011533000.1:c.1606A>T (TTC7A) XP_011531302.1:p.Ser536Cys
XM_011533001.1:c.1339A>T (TTC7A) XP_011531303.1:p.Ser447Cys
XM_005264439.4:c.2029A>T (TTC7A) XP_005264496.1:p.Ser677Cys
XM_011532998.3:c.2029A>T (TTC7A) XP_011531300.1:p.Ser677Cys
XM_011533000.3:c.1606A>T (TTC7A) XP_011531302.1:p.Ser536Cys
XM_011533001.3:c.1339A>T (TTC7A) XP_011531303.1:p.Ser447Cys
XM_017004524.1:c.2269A>T (TTC7A) XP_016860013.1:p.Ser757Cys
XM_017004525.1:c.2218A>T (TTC7A) XP_016860014.1:p.Ser740Cys
XM_017004526.1:c.2137A>T (TTC7A) XP_016860015.1:p.Ser713Cys
XM_024453013.1:c.1351A>T (TTC7A) XP_024308781.1:p.Ser451Cys
NM_020458.4:c.2386A>T (TTC7A) MANE Select NP_065191.2:p.Ser796Cys
NM_001288951.2:c.2458A>T (TTC7A) NP_001275880.1:p.Ser820Cys
NM_001288953.2:c.2284A>T (TTC7A) NP_001275882.1:p.Ser762Cys
NM_001288955.2:c.1324A>T (TTC7A) NP_001275884.1:p.Ser442Cys