Canonical Allele Identifier: CA346717523

Gene: TTC7A STPG4

Linked Data

• MyVariant Identifiers: chr2:g.47300872G>C (hg19) ; chr2:g.47073733G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47073733G>C , CM000664.2:g.47073733G>C	GRCh38
NC_000002.11:g.47300872G>C , CM000664.1:g.47300872G>C	GRCh37
NC_000002.10:g.47154376G>C	NCBI36
NG_034143.1:g.162605G>C
NG_034143.2:g.162605G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698500.1:n.4220G>C (TTC7A)
ENST00000698503.1:n.2393G>C (TTC7A)
ENST00000698504.1:n.468G>C (TTC7A)
ENST00000319190.11:c.2387G>C (TTC7A) MANE Select	ENSP00000316699.5:p.Ser796Thr
ENST00000651101.1:n.985G>C (TTC7A)
ENST00000651415.1:n.1178G>C (TTC7A)
ENST00000652236.1:n.1088G>C (TTC7A)
ENST00000652568.1:n.1060G>C (TTC7A)
ENST00000319190.9:c.2387G>C (TTC7A)	ENSP00000316699.5:p.Ser796Thr
ENST00000394850.6:c.2459G>C (TTC7A)	ENSP00000378320.2:p.Ser820Thr
ENST00000409245.5:c.2285G>C (TTC7A)	ENSP00000386307.1:p.Ser762Thr
ENST00000409825.5:c.2335G>C (TTC7A)
ENST00000422269.1:c.787-7596C>G
ENST00000441914.5:c.2228G>C (TTC7A)
ENST00000464527.2:n.399-7596C>G (STPG4)
ENST00000482548.1:n.402-5177C>G (STPG4)
ENST00000484061.5:n.1494G>C (TTC7A)
ENST00000491786.5:n.1791G>C (TTC7A)
ENST00000496939.1:n.416-26814C>G (STPG4)
NM_001288951.1:c.2459G>C (TTC7A)	NP_001275880.1:p.Ser820Thr
NM_001288953.1:c.2285G>C (TTC7A)	NP_001275882.1:p.Ser762Thr
NM_001288955.1:c.1325G>C (TTC7A)	NP_001275884.1:p.Ser442Thr
NM_020458.3:c.2387G>C (TTC7A)	NP_065191.2:p.Ser796Thr
XM_005264439.2:c.2030G>C (TTC7A)	XP_005264496.1:p.Ser677Thr
XM_011532998.1:c.2030G>C (TTC7A)	XP_011531300.1:p.Ser677Thr
XM_011533000.1:c.1607G>C (TTC7A)	XP_011531302.1:p.Ser536Thr
XM_011533001.1:c.1340G>C (TTC7A)	XP_011531303.1:p.Ser447Thr
XM_005264439.4:c.2030G>C (TTC7A)	XP_005264496.1:p.Ser677Thr
XM_011532998.3:c.2030G>C (TTC7A)	XP_011531300.1:p.Ser677Thr
XM_011533000.3:c.1607G>C (TTC7A)	XP_011531302.1:p.Ser536Thr
XM_011533001.3:c.1340G>C (TTC7A)	XP_011531303.1:p.Ser447Thr
XM_017004524.1:c.2270G>C (TTC7A)	XP_016860013.1:p.Ser757Thr
XM_017004525.1:c.2219G>C (TTC7A)	XP_016860014.1:p.Ser740Thr
XM_017004526.1:c.2138G>C (TTC7A)	XP_016860015.1:p.Ser713Thr
XM_024453013.1:c.1352G>C (TTC7A)	XP_024308781.1:p.Ser451Thr
NM_020458.4:c.2387G>C (TTC7A) MANE Select	NP_065191.2:p.Ser796Thr
NM_001288951.2:c.2459G>C (TTC7A)	NP_001275880.1:p.Ser820Thr
NM_001288953.2:c.2285G>C (TTC7A)	NP_001275882.1:p.Ser762Thr
NM_001288955.2:c.1325G>C (TTC7A)	NP_001275884.1:p.Ser442Thr