Canonical Allele Identifier: CA346718933

Gene: TTC7A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.46956989G>T , CM000664.2:g.46956989G>T	GRCh38
NC_000002.11:g.47184128G>T , CM000664.1:g.47184128G>T	GRCh37
NC_000002.10:g.47037632G>T	NCBI36
NG_034143.1:g.45861G>T
NG_034143.2:g.45861G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020458.4:c.499G>T MANE Select	NP_065191.2:p.Glu167Ter
ENST00000319190.11:c.499G>T MANE Select	ENSP00000316699.5:p.Glu167Ter
NM_001288951.1:c.499G>T	NP_001275880.1:p.Glu167Ter
NM_001288951.2:c.499G>T	NP_001275880.1:p.Glu167Ter
NM_001288953.1:c.397G>T	NP_001275882.1:p.Glu133Ter
NM_001288953.2:c.397G>T	NP_001275882.1:p.Glu133Ter
NM_001288955.1:c.-406G>T	NP_001275884.1:n.-406G>T
NM_001288955.2:c.-406G>T	NP_001275884.1:n.-406G>T
NM_020458.3:c.499G>T	NP_065191.2:p.Glu167Ter
ENST00000319190.9:c.499G>T	ENSP00000316699.5:p.Glu167Ter
ENST00000394850.6:c.499G>T	ENSP00000378320.2:p.Glu167Ter
ENST00000409245.5:c.397G>T	ENSP00000386307.1:p.Glu133Ter
ENST00000409825.5:c.389G>T
ENST00000441914.5:c.498G>T
ENST00000461601.5:n.766G>T
ENST00000698500.1:n.1446G>T
XM_005264439.2:c.84G>T	XP_005264496.1:p.Arg28=
XM_005264439.4:c.84G>T	XP_005264496.1:p.Arg28=
XM_011532998.1:c.84G>T	XP_011531300.1:p.Arg28=
XM_011532998.3:c.84G>T	XP_011531300.1:p.Arg28=
XM_011532999.1:c.499G>T	XP_011531301.1:p.Glu167Ter
XM_011532999.2:c.499G>T	XP_011531301.1:p.Glu167Ter
XM_017004524.1:c.499G>T	XP_016860013.1:p.Glu167Ter
XM_017004525.1:c.331G>T	XP_016860014.1:p.Glu111Ter
XM_017004526.1:c.499G>T	XP_016860015.1:p.Glu167Ter
XM_017004529.1:c.499G>T	XP_016860018.1:p.Glu167Ter
XR_001738853.2:n.811G>T
XR_001738854.1:n.810G>T
XR_939696.1:n.804G>T