Canonical Allele Identifier: CA46619105

Gene: TTC7A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46994416G>A , CM000664.2:g.46994416G>A	GRCh38
NC_000002.11:g.47221555G>A , CM000664.1:g.47221555G>A	GRCh37
NC_000002.10:g.47075059G>A	NCBI36
NG_034143.1:g.83288G>A
NG_034143.2:g.83288G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020458.4:c.903G>A MANE Select	NP_065191.2:p.Trp301Ter
ENST00000319190.11:c.903G>A MANE Select	ENSP00000316699.5:p.Trp301Ter
NM_001288951.1:c.903G>A	NP_001275880.1:p.Trp301Ter
NM_001288951.2:c.903G>A	NP_001275880.1:p.Trp301Ter
NM_001288953.1:c.801G>A	NP_001275882.1:p.Trp267Ter
NM_001288953.2:c.801G>A	NP_001275882.1:p.Trp267Ter
NM_001288955.1:c.-61-720G>A	NP_001275884.1:n.-61-720G>A
NM_001288955.2:c.-61-720G>A	NP_001275884.1:n.-61-720G>A
NM_020458.3:c.903G>A	NP_065191.2:p.Trp301Ter
ENST00000319190.9:c.903G>A	ENSP00000316699.5:p.Trp301Ter
ENST00000394850.6:c.903G>A	ENSP00000378320.2:p.Trp301Ter
ENST00000409245.5:c.801G>A	ENSP00000386307.1:p.Trp267Ter
ENST00000409825.5:c.851G>A
ENST00000441914.5:c.843-720G>A
ENST00000461601.5:n.1228G>A
ENST00000474321.6:n.387G>A
ENST00000484061.5:n.186G>A
ENST00000491786.5:n.307G>A
ENST00000698500.1:n.2736G>A
XM_005264439.2:c.546G>A	XP_005264496.1:p.Trp182Ter
XM_005264439.4:c.546G>A	XP_005264496.1:p.Trp182Ter
XM_011532998.1:c.546G>A	XP_011531300.1:p.Trp182Ter
XM_011532998.3:c.546G>A	XP_011531300.1:p.Trp182Ter
XM_011532999.1:c.903G>A	XP_011531301.1:p.Trp301Ter
XM_011532999.2:c.903G>A	XP_011531301.1:p.Trp301Ter
XM_011533000.1:c.123G>A	XP_011531302.1:p.Trp41Ter
XM_011533000.3:c.123G>A	XP_011531302.1:p.Trp41Ter
XM_017004524.1:c.903G>A	XP_016860013.1:p.Trp301Ter
XM_017004525.1:c.735G>A	XP_016860014.1:p.Trp245Ter
XM_017004526.1:c.903G>A	XP_016860015.1:p.Trp301Ter
XM_017004529.1:c.903G>A	XP_016860018.1:p.Trp301Ter
XR_001738853.2:n.1215G>A
XR_001738854.1:n.1214G>A
XR_939696.1:n.1208G>A