Canonical Allele Identifier: CA2495644220

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47074162T= , CM000664.2:g.47074162T= GRCh38
NC_000002.11:g.47301301T= , CM000664.1:g.47301301T= GRCh37
NC_000002.10:g.47154805T= NCBI36
NG_034143.1:g.163034T=
NG_034143.2:g.163034T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698500.1:n.4649T= (TTC7A)
ENST00000698503.1:n.2822T= (TTC7A)
ENST00000319190.11:c.*239T= (TTC7A) MANE Select ENSP00000316699.5:n.*239T=
ENST00000651101.1:n.1414T= (TTC7A)
ENST00000651415.1:n.1607T= (TTC7A)
ENST00000652236.1:n.1517T= (TTC7A)
ENST00000652568.1:n.1489T= (TTC7A)
ENST00000319190.9:c.*239T= (TTC7A) ENSP00000316699.5:n.*239T=
ENST00000394850.6:c.*239T= (TTC7A) ENSP00000378320.2:n.*239T=
ENST00000409825.5:c.2764T= (TTC7A)
ENST00000422269.1:c.787-8025A=
ENST00000464527.2:n.399-8025A= (STPG4)
ENST00000482548.1:n.402-5606A= (STPG4)
ENST00000484061.5:n.1923T= (TTC7A)
ENST00000491786.5:n.2220T= (TTC7A)
ENST00000496939.1:n.416-27243A= (STPG4)
NM_001288951.1:c.*239T= (TTC7A) NP_001275880.1:n.*239T=
NM_001288953.1:c.*239T= (TTC7A) NP_001275882.1:n.*239T=
NM_001288955.1:c.*239T= (TTC7A) NP_001275884.1:n.*239T=
NM_020458.3:c.*239T= (TTC7A) NP_065191.2:n.*239T=
XM_005264439.2:c.*239T= (TTC7A) XP_005264496.1:n.*239T=
XM_011532998.1:c.*239T= (TTC7A) XP_011531300.1:n.*239T=
XM_011533000.1:c.*239T= (TTC7A) XP_011531302.1:n.*239T=
XM_011533001.1:c.*239T= (TTC7A) XP_011531303.1:n.*239T=
XM_005264439.4:c.*239T= (TTC7A) XP_005264496.1:n.*239T=
XM_011532998.3:c.*239T= (TTC7A) XP_011531300.1:n.*239T=
XM_011533000.3:c.*239T= (TTC7A) XP_011531302.1:n.*239T=
XM_011533001.3:c.*239T= (TTC7A) XP_011531303.1:n.*239T=
XM_017004524.1:c.*239T= (TTC7A) XP_016860013.1:n.*239T=
XM_017004525.1:c.*239T= (TTC7A) XP_016860014.1:n.*239T=
XM_017004526.1:c.*239T= (TTC7A) XP_016860015.1:n.*239T=
XM_024453013.1:c.*239T= (TTC7A) XP_024308781.1:n.*239T=
NM_020458.4:c.*239T= (TTC7A) MANE Select NP_065191.2:n.*239T=
NM_001288951.2:c.*239T= (TTC7A) NP_001275880.1:n.*239T=
NM_001288953.2:c.*239T= (TTC7A) NP_001275882.1:n.*239T=
NM_001288955.2:c.*239T= (TTC7A) NP_001275884.1:n.*239T=