Canonical Allele Identifier: CA2495643901

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47073674C= , CM000664.2:g.47073674C= GRCh38
NC_000002.11:g.47300813C= , CM000664.1:g.47300813C= GRCh37
NC_000002.10:g.47154317C= NCBI36
NG_034143.1:g.162546C=
NG_034143.2:g.162546C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698500.1:n.4189-28C= (TTC7A)
ENST00000698503.1:n.2362-28C= (TTC7A)
ENST00000698504.1:n.437-28C= (TTC7A)
ENST00000319190.11:c.2356-28C= (TTC7A) MANE Select ENSP00000316699.5:n.2356-28C=
ENST00000651101.1:n.954-28C= (TTC7A)
ENST00000651415.1:n.1147-28C= (TTC7A)
ENST00000652236.1:n.1057-28C= (TTC7A)
ENST00000652568.1:n.1029-28C= (TTC7A)
ENST00000319190.9:c.2356-28C= (TTC7A) ENSP00000316699.5:n.2356-28C=
ENST00000394850.6:c.2428-28C= (TTC7A) ENSP00000378320.2:n.2428-28C=
ENST00000409245.5:c.2254-28C= (TTC7A) ENSP00000386307.1:n.2254-28C=
ENST00000409825.5:c.2304-28C= (TTC7A)
ENST00000422269.1:c.787-7537G=
ENST00000441914.5:c.2197-28C= (TTC7A)
ENST00000464527.2:n.399-7537G= (STPG4)
ENST00000482548.1:n.402-5118G= (STPG4)
ENST00000484061.5:n.1463-28C= (TTC7A)
ENST00000491786.5:n.1760-28C= (TTC7A)
ENST00000496939.1:n.416-26755G= (STPG4)
NM_001288951.1:c.2428-28C= (TTC7A) NP_001275880.1:n.2428-28C=
NM_001288953.1:c.2254-28C= (TTC7A) NP_001275882.1:n.2254-28C=
NM_001288955.1:c.1294-28C= (TTC7A) NP_001275884.1:n.1294-28C=
NM_020458.3:c.2356-28C= (TTC7A) NP_065191.2:n.2356-28C=
XM_005264439.2:c.1999-28C= (TTC7A) XP_005264496.1:n.1999-28C=
XM_011532998.1:c.1999-28C= (TTC7A) XP_011531300.1:n.1999-28C=
XM_011533000.1:c.1576-28C= (TTC7A) XP_011531302.1:n.1576-28C=
XM_011533001.1:c.1309-28C= (TTC7A) XP_011531303.1:n.1309-28C=
XM_005264439.4:c.1999-28C= (TTC7A) XP_005264496.1:n.1999-28C=
XM_011532998.3:c.1999-28C= (TTC7A) XP_011531300.1:n.1999-28C=
XM_011533000.3:c.1576-28C= (TTC7A) XP_011531302.1:n.1576-28C=
XM_011533001.3:c.1309-28C= (TTC7A) XP_011531303.1:n.1309-28C=
XM_017004524.1:c.2239-28C= (TTC7A) XP_016860013.1:n.2239-28C=
XM_017004525.1:c.2188-28C= (TTC7A) XP_016860014.1:n.2188-28C=
XM_017004526.1:c.2107-28C= (TTC7A) XP_016860015.1:n.2107-28C=
XM_024453013.1:c.1321-28C= (TTC7A) XP_024308781.1:n.1321-28C=
NM_020458.4:c.2356-28C= (TTC7A) MANE Select NP_065191.2:n.2356-28C=
NM_001288951.2:c.2428-28C= (TTC7A) NP_001275880.1:n.2428-28C=
NM_001288953.2:c.2254-28C= (TTC7A) NP_001275882.1:n.2254-28C=
NM_001288955.2:c.1294-28C= (TTC7A) NP_001275884.1:n.1294-28C=