Canonical Allele Identifier: CA2749789005

Gene: TTC7A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47002512_47002513insC , CM000664.2:g.47002512_47002513insC	GRCh38
NC_000002.11:g.47229651_47229652insC , CM000664.1:g.47229651_47229652insC	GRCh37
NC_000002.10:g.47083155_47083156insC	NCBI36
NG_034143.1:g.91384_91385insC
NG_034143.2:g.91384_91385insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000698500.1:n.2899-3410_2899-3409insC
ENST00000319190.11:c.1066-3410_1066-3409insC MANE Select	ENSP00000316699.5:n.1066-3410_1066-3409insC
ENST00000319190.9:c.1066-3410_1066-3409insC	ENSP00000316699.5:n.1066-3410_1066-3409insC
ENST00000394850.6:c.1066-3410_1066-3409insC	ENSP00000378320.2:n.1066-3410_1066-3409insC
ENST00000409245.5:c.964-3410_964-3409insC	ENSP00000386307.1:n.964-3410_964-3409insC
ENST00000409825.5:c.1014-3410_1014-3409insC
ENST00000441914.5:c.907-3410_907-3409insC
ENST00000461601.5:n.1391-3410_1391-3409insC
ENST00000474321.6:n.550-3410_550-3409insC
ENST00000484061.5:n.349-3410_349-3409insC
ENST00000491786.5:n.470-3410_470-3409insC
NM_001288951.1:c.1066-3410_1066-3409insC	NP_001275880.1:n.1066-3410_1066-3409insC
NM_001288953.1:c.964-3410_964-3409insC	NP_001275882.1:n.964-3410_964-3409insC
NM_001288955.1:c.4-3410_4-3409insC	NP_001275884.1:n.4-3410_4-3409insC
NM_020458.3:c.1066-3410_1066-3409insC	NP_065191.2:n.1066-3410_1066-3409insC
XM_005264439.2:c.709-3410_709-3409insC	XP_005264496.1:n.709-3410_709-3409insC
XM_011532998.1:c.709-3410_709-3409insC	XP_011531300.1:n.709-3410_709-3409insC
XM_011532999.1:c.1066-3410_1066-3409insC	XP_011531301.1:n.1066-3410_1066-3409insC
XM_011533000.1:c.286-3410_286-3409insC	XP_011531302.1:n.286-3410_286-3409insC
XR_939696.1:n.1371-3410_1371-3409insC
XM_005264439.4:c.709-3410_709-3409insC	XP_005264496.1:n.709-3410_709-3409insC
XM_011532998.3:c.709-3410_709-3409insC	XP_011531300.1:n.709-3410_709-3409insC
XM_011532999.2:c.1066-3410_1066-3409insC	XP_011531301.1:n.1066-3410_1066-3409insC
XM_011533000.3:c.286-3410_286-3409insC	XP_011531302.1:n.286-3410_286-3409insC
XM_017004524.1:c.1066-3410_1066-3409insC	XP_016860013.1:n.1066-3410_1066-3409insC
XM_017004525.1:c.898-3410_898-3409insC	XP_016860014.1:n.898-3410_898-3409insC
XM_017004526.1:c.1066-3410_1066-3409insC	XP_016860015.1:n.1066-3410_1066-3409insC
XM_017004529.1:c.1066-3410_1066-3409insC	XP_016860018.1:n.1066-3410_1066-3409insC
XM_024453013.1:c.31-3410_31-3409insC	XP_024308781.1:n.31-3410_31-3409insC
XR_001738853.2:n.1378-3410_1378-3409insC
XR_001738854.1:n.1377-3410_1377-3409insC
NM_020458.4:c.1066-3410_1066-3409insC MANE Select	NP_065191.2:n.1066-3410_1066-3409insC
NM_001288951.2:c.1066-3410_1066-3409insC	NP_001275880.1:n.1066-3410_1066-3409insC
NM_001288953.2:c.964-3410_964-3409insC	NP_001275882.1:n.964-3410_964-3409insC
NM_001288955.2:c.4-3410_4-3409insC	NP_001275884.1:n.4-3410_4-3409insC