Canonical Allele Identifier: CA346716450

Gene: TTC7A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47024360G>A , CM000664.2:g.47024360G>A	GRCh38
NC_000002.11:g.47251499G>A , CM000664.1:g.47251499G>A	GRCh37
NC_000002.10:g.47105003G>A	NCBI36
NG_034143.1:g.113232G>A
NG_034143.2:g.113232G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020458.4:c.1641+1G>A MANE Select	NP_065191.2:n.1641+1G>A
ENST00000319190.11:c.1641+1G>A MANE Select	ENSP00000316699.5:n.1641+1G>A
NM_001288951.1:c.1641+1G>A	NP_001275880.1:n.1641+1G>A
NM_001288951.2:c.1641+1G>A	NP_001275880.1:n.1641+1G>A
NM_001288953.1:c.1539+1G>A	NP_001275882.1:n.1539+1G>A
NM_001288953.2:c.1539+1G>A	NP_001275882.1:n.1539+1G>A
NM_001288955.1:c.579+1G>A	NP_001275884.1:n.579+1G>A
NM_001288955.2:c.579+1G>A	NP_001275884.1:n.579+1G>A
NM_020458.3:c.1641+1G>A	NP_065191.2:n.1641+1G>A
ENST00000319190.9:c.1641+1G>A	ENSP00000316699.5:n.1641+1G>A
ENST00000394850.6:c.1641+1G>A	ENSP00000378320.2:n.1641+1G>A
ENST00000409245.5:c.1539+1G>A	ENSP00000386307.1:n.1539+1G>A
ENST00000409825.5:c.1589+1G>A
ENST00000440051.1:c.448+1G>A
ENST00000441914.5:c.1482+1G>A
ENST00000461601.5:n.1966+1G>A
ENST00000484061.5:n.748+1G>A
ENST00000491786.5:n.1045+1G>A
ENST00000651101.1:n.589+1G>A
ENST00000651415.1:n.432+1G>A
ENST00000652236.1:n.342+1G>A
ENST00000652568.1:n.314+1G>A
ENST00000698500.1:n.3474+1G>A
XM_005264439.2:c.1284+1G>A	XP_005264496.1:n.1284+1G>A
XM_005264439.4:c.1284+1G>A	XP_005264496.1:n.1284+1G>A
XM_011532998.1:c.1284+1G>A	XP_011531300.1:n.1284+1G>A
XM_011532998.3:c.1284+1G>A	XP_011531300.1:n.1284+1G>A
XM_011532999.1:c.1641+1G>A	XP_011531301.1:n.1641+1G>A
XM_011532999.2:c.1641+1G>A	XP_011531301.1:n.1641+1G>A
XM_011533000.1:c.861+1G>A	XP_011531302.1:n.861+1G>A
XM_011533000.3:c.861+1G>A	XP_011531302.1:n.861+1G>A
XM_011533001.1:c.594+1G>A	XP_011531303.1:n.594+1G>A
XM_011533001.3:c.594+1G>A	XP_011531303.1:n.594+1G>A
XM_017004524.1:c.1641+1G>A	XP_016860013.1:n.1641+1G>A
XM_017004525.1:c.1473+1G>A	XP_016860014.1:n.1473+1G>A
XM_017004526.1:c.1393-4864G>A	XP_016860015.1:n.1393-4864G>A
XM_017004529.1:c.1641+1G>A	XP_016860018.1:n.1641+1G>A
XM_024453013.1:c.606+1G>A	XP_024308781.1:n.606+1G>A
XR_001738853.2:n.1953+1G>A
XR_001738854.1:n.1834+1G>A
XR_939696.1:n.1946+1G>A