Canonical Allele Identifier: CA2504462386

Gene: TTC7A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47002562_47002649del , CM000664.2:g.47002562_47002649del	GRCh38
NC_000002.11:g.47229701_47229788del , CM000664.1:g.47229701_47229788del	GRCh37
NC_000002.10:g.47083205_47083292del	NCBI36
NG_034143.1:g.91434_91521del
NG_034143.2:g.91434_91521del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698500.1:n.2899-3360_2899-3273del
ENST00000319190.11:c.1066-3360_1066-3273del MANE Select	ENSP00000316699.5:n.1066-3360_1066-3273del
ENST00000319190.9:c.1066-3360_1066-3273del	ENSP00000316699.5:n.1066-3360_1066-3273del
ENST00000394850.6:c.1066-3360_1066-3273del	ENSP00000378320.2:n.1066-3360_1066-3273del
ENST00000409245.5:c.964-3360_964-3273del	ENSP00000386307.1:n.964-3360_964-3273del
ENST00000409825.5:c.1014-3360_1014-3273del
ENST00000441914.5:c.907-3360_907-3273del
ENST00000461601.5:n.1391-3360_1391-3273del
ENST00000474321.6:n.550-3360_550-3273del
ENST00000484061.5:n.349-3360_349-3273del
ENST00000491786.5:n.470-3360_470-3273del
NM_001288951.1:c.1066-3360_1066-3273del	NP_001275880.1:n.1066-3360_1066-3273del
NM_001288953.1:c.964-3360_964-3273del	NP_001275882.1:n.964-3360_964-3273del
NM_001288955.1:c.4-3360_4-3273del	NP_001275884.1:n.4-3360_4-3273del
NM_020458.3:c.1066-3360_1066-3273del	NP_065191.2:n.1066-3360_1066-3273del
XM_005264439.2:c.709-3360_709-3273del	XP_005264496.1:n.709-3360_709-3273del
XM_011532998.1:c.709-3360_709-3273del	XP_011531300.1:n.709-3360_709-3273del
XM_011532999.1:c.1066-3360_1066-3273del	XP_011531301.1:n.1066-3360_1066-3273del
XM_011533000.1:c.286-3360_286-3273del	XP_011531302.1:n.286-3360_286-3273del
XR_939696.1:n.1371-3360_1371-3273del
XM_005264439.4:c.709-3360_709-3273del	XP_005264496.1:n.709-3360_709-3273del
XM_011532998.3:c.709-3360_709-3273del	XP_011531300.1:n.709-3360_709-3273del
XM_011532999.2:c.1066-3360_1066-3273del	XP_011531301.1:n.1066-3360_1066-3273del
XM_011533000.3:c.286-3360_286-3273del	XP_011531302.1:n.286-3360_286-3273del
XM_017004524.1:c.1066-3360_1066-3273del	XP_016860013.1:n.1066-3360_1066-3273del
XM_017004525.1:c.898-3360_898-3273del	XP_016860014.1:n.898-3360_898-3273del
XM_017004526.1:c.1066-3360_1066-3273del	XP_016860015.1:n.1066-3360_1066-3273del
XM_017004529.1:c.1066-3360_1066-3273del	XP_016860018.1:n.1066-3360_1066-3273del
XM_024453013.1:c.31-3360_31-3273del	XP_024308781.1:n.31-3360_31-3273del
XR_001738853.2:n.1378-3360_1378-3273del
XR_001738854.1:n.1377-3360_1377-3273del
NM_020458.4:c.1066-3360_1066-3273del MANE Select	NP_065191.2:n.1066-3360_1066-3273del
NM_001288951.2:c.1066-3360_1066-3273del	NP_001275880.1:n.1066-3360_1066-3273del
NM_001288953.2:c.964-3360_964-3273del	NP_001275882.1:n.964-3360_964-3273del
NM_001288955.2:c.4-3360_4-3273del	NP_001275884.1:n.4-3360_4-3273del