Canonical Allele Identifier: CA2495643995

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47073833C= , CM000664.2:g.47073833C= GRCh38
NC_000002.11:g.47300972C= , CM000664.1:g.47300972C= GRCh37
NC_000002.10:g.47154476C= NCBI36
NG_034143.1:g.162705C=
NG_034143.2:g.162705C=

Transcript Alleles

HGVS Amino-acid change
ENST00000698500.1:n.4320C= (TTC7A)
ENST00000698503.1:n.2493C= (TTC7A)
ENST00000319190.11:c.2487C= (TTC7A) MANE Select ENSP00000316699.5:p.Asn829=
ENST00000651101.1:n.1085C= (TTC7A)
ENST00000651415.1:n.1278C= (TTC7A)
ENST00000652236.1:n.1188C= (TTC7A)
ENST00000652568.1:n.1160C= (TTC7A)
ENST00000319190.9:c.2487C= (TTC7A) ENSP00000316699.5:p.Asn829=
ENST00000394850.6:c.2559C= (TTC7A) ENSP00000378320.2:p.Asn853=
ENST00000409245.5:c.2385C= (TTC7A) ENSP00000386307.1:p.Asn795=
ENST00000409825.5:c.2435C= (TTC7A)
ENST00000422269.1:c.787-7696G=
ENST00000441914.5:c.2328C= (TTC7A)
ENST00000464527.2:n.399-7696G= (STPG4)
ENST00000482548.1:n.402-5277G= (STPG4)
ENST00000484061.5:n.1594C= (TTC7A)
ENST00000491786.5:n.1891C= (TTC7A)
ENST00000496939.1:n.416-26914G= (STPG4)
NM_001288951.1:c.2559C= (TTC7A) NP_001275880.1:p.Asn853=
NM_001288953.1:c.2385C= (TTC7A) NP_001275882.1:p.Asn795=
NM_001288955.1:c.1425C= (TTC7A) NP_001275884.1:p.Asn475=
NM_020458.3:c.2487C= (TTC7A) NP_065191.2:p.Asn829=
XM_005264439.2:c.2130C= (TTC7A) XP_005264496.1:p.Asn710=
XM_011532998.1:c.2130C= (TTC7A) XP_011531300.1:p.Asn710=
XM_011533000.1:c.1707C= (TTC7A) XP_011531302.1:p.Asn569=
XM_011533001.1:c.1440C= (TTC7A) XP_011531303.1:p.Asn480=
XM_005264439.4:c.2130C= (TTC7A) XP_005264496.1:p.Asn710=
XM_011532998.3:c.2130C= (TTC7A) XP_011531300.1:p.Asn710=
XM_011533000.3:c.1707C= (TTC7A) XP_011531302.1:p.Asn569=
XM_011533001.3:c.1440C= (TTC7A) XP_011531303.1:p.Asn480=
XM_017004524.1:c.2370C= (TTC7A) XP_016860013.1:p.Asn790=
XM_017004525.1:c.2319C= (TTC7A) XP_016860014.1:p.Asn773=
XM_017004526.1:c.2238C= (TTC7A) XP_016860015.1:p.Asn746=
XM_024453013.1:c.1452C= (TTC7A) XP_024308781.1:p.Asn484=
NM_020458.4:c.2487C= (TTC7A) MANE Select NP_065191.2:p.Asn829=
NM_001288951.2:c.2559C= (TTC7A) NP_001275880.1:p.Asn853=
NM_001288953.2:c.2385C= (TTC7A) NP_001275882.1:p.Asn795=
NM_001288955.2:c.1425C= (TTC7A) NP_001275884.1:p.Asn475=