Canonical Allele Identifier: CA2495643919

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47073706T= , CM000664.2:g.47073706T= GRCh38
NC_000002.11:g.47300845T= , CM000664.1:g.47300845T= GRCh37
NC_000002.10:g.47154349T= NCBI36
NG_034143.1:g.162578T=
NG_034143.2:g.162578T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698500.1:n.4193T= (TTC7A)
ENST00000698503.1:n.2366T= (TTC7A)
ENST00000698504.1:n.441T= (TTC7A)
ENST00000319190.11:c.2360T= (TTC7A) MANE Select ENSP00000316699.5:p.Leu787=
ENST00000651101.1:n.958T= (TTC7A)
ENST00000651415.1:n.1151T= (TTC7A)
ENST00000652236.1:n.1061T= (TTC7A)
ENST00000652568.1:n.1033T= (TTC7A)
ENST00000319190.9:c.2360T= (TTC7A) ENSP00000316699.5:p.Leu787=
ENST00000394850.6:c.2432T= (TTC7A) ENSP00000378320.2:p.Leu811=
ENST00000409245.5:c.2258T= (TTC7A) ENSP00000386307.1:p.Leu753=
ENST00000409825.5:c.2308T= (TTC7A)
ENST00000422269.1:c.787-7569A=
ENST00000441914.5:c.2201T= (TTC7A)
ENST00000464527.2:n.399-7569A= (STPG4)
ENST00000482548.1:n.402-5150A= (STPG4)
ENST00000484061.5:n.1467T= (TTC7A)
ENST00000491786.5:n.1764T= (TTC7A)
ENST00000496939.1:n.416-26787A= (STPG4)
NM_001288951.1:c.2432T= (TTC7A) NP_001275880.1:p.Leu811=
NM_001288953.1:c.2258T= (TTC7A) NP_001275882.1:p.Leu753=
NM_001288955.1:c.1298T= (TTC7A) NP_001275884.1:p.Leu433=
NM_020458.3:c.2360T= (TTC7A) NP_065191.2:p.Leu787=
XM_005264439.2:c.2003T= (TTC7A) XP_005264496.1:p.Leu668=
XM_011532998.1:c.2003T= (TTC7A) XP_011531300.1:p.Leu668=
XM_011533000.1:c.1580T= (TTC7A) XP_011531302.1:p.Leu527=
XM_011533001.1:c.1313T= (TTC7A) XP_011531303.1:p.Leu438=
XM_005264439.4:c.2003T= (TTC7A) XP_005264496.1:p.Leu668=
XM_011532998.3:c.2003T= (TTC7A) XP_011531300.1:p.Leu668=
XM_011533000.3:c.1580T= (TTC7A) XP_011531302.1:p.Leu527=
XM_011533001.3:c.1313T= (TTC7A) XP_011531303.1:p.Leu438=
XM_017004524.1:c.2243T= (TTC7A) XP_016860013.1:p.Leu748=
XM_017004525.1:c.2192T= (TTC7A) XP_016860014.1:p.Leu731=
XM_017004526.1:c.2111T= (TTC7A) XP_016860015.1:p.Leu704=
XM_024453013.1:c.1325T= (TTC7A) XP_024308781.1:p.Leu442=
NM_020458.4:c.2360T= (TTC7A) MANE Select NP_065191.2:p.Leu787=
NM_001288951.2:c.2432T= (TTC7A) NP_001275880.1:p.Leu811=
NM_001288953.2:c.2258T= (TTC7A) NP_001275882.1:p.Leu753=
NM_001288955.2:c.1298T= (TTC7A) NP_001275884.1:p.Leu433=