Canonical Allele Identifier: CA2580582988

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47073724_47073725insGCC , CM000664.2:g.47073724_47073725insGCC GRCh38
NC_000002.11:g.47300863_47300864insGCC , CM000664.1:g.47300863_47300864insGCC GRCh37
NC_000002.10:g.47154367_47154368insGCC NCBI36
NG_034143.1:g.162596_162597insGCC
NG_034143.2:g.162596_162597insGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000698500.1:n.4211_4212insGCC (TTC7A)
ENST00000698503.1:n.2384_2385insGCC (TTC7A)
ENST00000698504.1:n.459_460insGCC (TTC7A)
ENST00000319190.11:c.2378_2379insGCC (TTC7A) MANE Select ENSP00000316699.5:p.Gly793_His794insPro
ENST00000651101.1:n.976_977insGCC (TTC7A)
ENST00000651415.1:n.1169_1170insGCC (TTC7A)
ENST00000652236.1:n.1079_1080insGCC (TTC7A)
ENST00000652568.1:n.1051_1052insGCC (TTC7A)
ENST00000319190.9:c.2378_2379insGCC (TTC7A) ENSP00000316699.5:p.Gly793_His794insPro
ENST00000394850.6:c.2450_2451insGCC (TTC7A) ENSP00000378320.2:p.Gly817_His818insPro
ENST00000409245.5:c.2276_2277insGCC (TTC7A) ENSP00000386307.1:p.Gly759_His760insPro
ENST00000409825.5:c.2326_2327insGCC (TTC7A)
ENST00000422269.1:c.787-7588_787-7587insGGC
ENST00000441914.5:c.2219_2220insGCC (TTC7A)
ENST00000464527.2:n.399-7588_399-7587insGGC (STPG4)
ENST00000482548.1:n.402-5169_402-5168insGGC (STPG4)
ENST00000484061.5:n.1485_1486insGCC (TTC7A)
ENST00000491786.5:n.1782_1783insGCC (TTC7A)
ENST00000496939.1:n.416-26806_416-26805insGGC (STPG4)
NM_001288951.1:c.2450_2451insGCC (TTC7A) NP_001275880.1:p.Gly817_His818insPro
NM_001288953.1:c.2276_2277insGCC (TTC7A) NP_001275882.1:p.Gly759_His760insPro
NM_001288955.1:c.1316_1317insGCC (TTC7A) NP_001275884.1:p.Gly439_His440insPro
NM_020458.3:c.2378_2379insGCC (TTC7A) NP_065191.2:p.Gly793_His794insPro
XM_005264439.2:c.2021_2022insGCC (TTC7A) XP_005264496.1:p.Gly674_His675insPro
XM_011532998.1:c.2021_2022insGCC (TTC7A) XP_011531300.1:p.Gly674_His675insPro
XM_011533000.1:c.1598_1599insGCC (TTC7A) XP_011531302.1:p.Gly533_His534insPro
XM_011533001.1:c.1331_1332insGCC (TTC7A) XP_011531303.1:p.Gly444_His445insPro
XM_005264439.4:c.2021_2022insGCC (TTC7A) XP_005264496.1:p.Gly674_His675insPro
XM_011532998.3:c.2021_2022insGCC (TTC7A) XP_011531300.1:p.Gly674_His675insPro
XM_011533000.3:c.1598_1599insGCC (TTC7A) XP_011531302.1:p.Gly533_His534insPro
XM_011533001.3:c.1331_1332insGCC (TTC7A) XP_011531303.1:p.Gly444_His445insPro
XM_017004524.1:c.2261_2262insGCC (TTC7A) XP_016860013.1:p.Gly754_His755insPro
XM_017004525.1:c.2210_2211insGCC (TTC7A) XP_016860014.1:p.Gly737_His738insPro
XM_017004526.1:c.2129_2130insGCC (TTC7A) XP_016860015.1:p.Gly710_His711insPro
XM_024453013.1:c.1343_1344insGCC (TTC7A) XP_024308781.1:p.Gly448_His449insPro
NM_020458.4:c.2378_2379insGCC (TTC7A) MANE Select NP_065191.2:p.Gly793_His794insPro
NM_001288951.2:c.2450_2451insGCC (TTC7A) NP_001275880.1:p.Gly817_His818insPro
NM_001288953.2:c.2276_2277insGCC (TTC7A) NP_001275882.1:p.Gly759_His760insPro
NM_001288955.2:c.1316_1317insGCC (TTC7A) NP_001275884.1:p.Gly439_His440insPro