Canonical Allele Identifier: CA346717202

Gene: TTC7A STPG4

Linked Data

• MyVariant Identifiers: chr2:g.47300841G>C (hg19) ; chr2:g.47073702G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47073702G>C , CM000664.2:g.47073702G>C	GRCh38
NC_000002.11:g.47300841G>C , CM000664.1:g.47300841G>C	GRCh37
NC_000002.10:g.47154345G>C	NCBI36
NG_034143.1:g.162574G>C
NG_034143.2:g.162574G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698500.1:n.4189G>C (TTC7A)
ENST00000698503.1:n.2362G>C (TTC7A)
ENST00000698504.1:n.437G>C (TTC7A)
ENST00000319190.11:c.2356G>C (TTC7A) MANE Select	ENSP00000316699.5:p.Gly786Arg
ENST00000651101.1:n.954G>C (TTC7A)
ENST00000651415.1:n.1147G>C (TTC7A)
ENST00000652236.1:n.1057G>C (TTC7A)
ENST00000652568.1:n.1029G>C (TTC7A)
ENST00000319190.9:c.2356G>C (TTC7A)	ENSP00000316699.5:p.Gly786Arg
ENST00000394850.6:c.2428G>C (TTC7A)	ENSP00000378320.2:p.Gly810Arg
ENST00000409245.5:c.2254G>C (TTC7A)	ENSP00000386307.1:p.Gly752Arg
ENST00000409825.5:c.2304G>C (TTC7A)
ENST00000422269.1:c.787-7565C>G
ENST00000441914.5:c.2197G>C (TTC7A)
ENST00000464527.2:n.399-7565C>G (STPG4)
ENST00000482548.1:n.402-5146C>G (STPG4)
ENST00000484061.5:n.1463G>C (TTC7A)
ENST00000491786.5:n.1760G>C (TTC7A)
ENST00000496939.1:n.416-26783C>G (STPG4)
NM_001288951.1:c.2428G>C (TTC7A)	NP_001275880.1:p.Gly810Arg
NM_001288953.1:c.2254G>C (TTC7A)	NP_001275882.1:p.Gly752Arg
NM_001288955.1:c.1294G>C (TTC7A)	NP_001275884.1:p.Gly432Arg
NM_020458.3:c.2356G>C (TTC7A)	NP_065191.2:p.Gly786Arg
XM_005264439.2:c.1999G>C (TTC7A)	XP_005264496.1:p.Gly667Arg
XM_011532998.1:c.1999G>C (TTC7A)	XP_011531300.1:p.Gly667Arg
XM_011533000.1:c.1576G>C (TTC7A)	XP_011531302.1:p.Gly526Arg
XM_011533001.1:c.1309G>C (TTC7A)	XP_011531303.1:p.Gly437Arg
XM_005264439.4:c.1999G>C (TTC7A)	XP_005264496.1:p.Gly667Arg
XM_011532998.3:c.1999G>C (TTC7A)	XP_011531300.1:p.Gly667Arg
XM_011533000.3:c.1576G>C (TTC7A)	XP_011531302.1:p.Gly526Arg
XM_011533001.3:c.1309G>C (TTC7A)	XP_011531303.1:p.Gly437Arg
XM_017004524.1:c.2239G>C (TTC7A)	XP_016860013.1:p.Gly747Arg
XM_017004525.1:c.2188G>C (TTC7A)	XP_016860014.1:p.Gly730Arg
XM_017004526.1:c.2107G>C (TTC7A)	XP_016860015.1:p.Gly703Arg
XM_024453013.1:c.1321G>C (TTC7A)	XP_024308781.1:p.Gly441Arg
NM_020458.4:c.2356G>C (TTC7A) MANE Select	NP_065191.2:p.Gly786Arg
NM_001288951.2:c.2428G>C (TTC7A)	NP_001275880.1:p.Gly810Arg
NM_001288953.2:c.2254G>C (TTC7A)	NP_001275882.1:p.Gly752Arg
NM_001288955.2:c.1294G>C (TTC7A)	NP_001275884.1:p.Gly432Arg