Canonical Allele Identifier: CA2495604497

Gene: TTC7A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47002943_47002944delinsGC , CM000664.2:g.47002943_47002944delinsGC	GRCh38
NC_000002.11:g.47230082_47230083delinsGC , CM000664.1:g.47230082_47230083delinsGC	GRCh37
NC_000002.10:g.47083586_47083587delinsGC	NCBI36
NG_034143.1:g.91815_91816delinsGC
NG_034143.2:g.91815_91816delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698500.1:n.2899-2979_2899-2978delinsGC
ENST00000319190.11:c.1066-2979_1066-2978delinsGC MANE Select	ENSP00000316699.5:n.1066-2979_1066-2978delinsGC
ENST00000319190.9:c.1066-2979_1066-2978delinsGC	ENSP00000316699.5:n.1066-2979_1066-2978delinsGC
ENST00000394850.6:c.1066-2979_1066-2978delinsGC	ENSP00000378320.2:n.1066-2979_1066-2978delinsGC
ENST00000409245.5:c.964-2979_964-2978delinsGC	ENSP00000386307.1:n.964-2979_964-2978delinsGC
ENST00000409825.5:c.1014-2979_1014-2978delinsGC
ENST00000441914.5:c.907-2979_907-2978delinsGC
ENST00000461601.5:n.1391-2979_1391-2978delinsGC
ENST00000474321.6:n.550-2979_550-2978delinsGC
ENST00000484061.5:n.349-2979_349-2978delinsGC
ENST00000491786.5:n.470-2979_470-2978delinsGC
NM_001288951.1:c.1066-2979_1066-2978delinsGC	NP_001275880.1:n.1066-2979_1066-2978delinsGC
NM_001288953.1:c.964-2979_964-2978delinsGC	NP_001275882.1:n.964-2979_964-2978delinsGC
NM_001288955.1:c.4-2979_4-2978delinsGC	NP_001275884.1:n.4-2979_4-2978delinsGC
NM_020458.3:c.1066-2979_1066-2978delinsGC	NP_065191.2:n.1066-2979_1066-2978delinsGC
XM_005264439.2:c.709-2979_709-2978delinsGC	XP_005264496.1:n.709-2979_709-2978delinsGC
XM_011532998.1:c.709-2979_709-2978delinsGC	XP_011531300.1:n.709-2979_709-2978delinsGC
XM_011532999.1:c.1066-2979_1066-2978delinsGC	XP_011531301.1:n.1066-2979_1066-2978delinsGC
XM_011533000.1:c.286-2979_286-2978delinsGC	XP_011531302.1:n.286-2979_286-2978delinsGC
XR_939696.1:n.1371-2979_1371-2978delinsGC
XM_005264439.4:c.709-2979_709-2978delinsGC	XP_005264496.1:n.709-2979_709-2978delinsGC
XM_011532998.3:c.709-2979_709-2978delinsGC	XP_011531300.1:n.709-2979_709-2978delinsGC
XM_011532999.2:c.1066-2979_1066-2978delinsGC	XP_011531301.1:n.1066-2979_1066-2978delinsGC
XM_011533000.3:c.286-2979_286-2978delinsGC	XP_011531302.1:n.286-2979_286-2978delinsGC
XM_017004524.1:c.1066-2979_1066-2978delinsGC	XP_016860013.1:n.1066-2979_1066-2978delinsGC
XM_017004525.1:c.898-2979_898-2978delinsGC	XP_016860014.1:n.898-2979_898-2978delinsGC
XM_017004526.1:c.1066-2979_1066-2978delinsGC	XP_016860015.1:n.1066-2979_1066-2978delinsGC
XM_017004529.1:c.1066-2979_1066-2978delinsGC	XP_016860018.1:n.1066-2979_1066-2978delinsGC
XM_024453013.1:c.31-2979_31-2978delinsGC	XP_024308781.1:n.31-2979_31-2978delinsGC
XR_001738853.2:n.1378-2979_1378-2978delinsGC
XR_001738854.1:n.1377-2979_1377-2978delinsGC
NM_020458.4:c.1066-2979_1066-2978delinsGC MANE Select	NP_065191.2:n.1066-2979_1066-2978delinsGC
NM_001288951.2:c.1066-2979_1066-2978delinsGC	NP_001275880.1:n.1066-2979_1066-2978delinsGC
NM_001288953.2:c.964-2979_964-2978delinsGC	NP_001275882.1:n.964-2979_964-2978delinsGC
NM_001288955.2:c.4-2979_4-2978delinsGC	NP_001275884.1:n.4-2979_4-2978delinsGC