Canonical Allele Identifier: CA2495604533

Gene: TTC7A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47002985_47002997delinsTGCTGCTGCTGCC , CM000664.2:g.47002985_47002997delinsTGCTGCTGCTGCC	GRCh38
NC_000002.11:g.47230124_47230136delinsTGCTGCTGCTGCC , CM000664.1:g.47230124_47230136delinsTGCTGCTGCTGCC	GRCh37
NC_000002.10:g.47083628_47083640delinsTGCTGCTGCTGCC	NCBI36
NG_034143.1:g.91857_91869delinsTGCTGCTGCTGCC
NG_034143.2:g.91857_91869delinsTGCTGCTGCTGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698500.1:n.2899-2937_2899-2925delinsTGCTGCTGCTGCC
ENST00000319190.11:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC MANE Select	ENSP00000316699.5:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
ENST00000319190.9:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC	ENSP00000316699.5:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
ENST00000394850.6:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC	ENSP00000378320.2:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
ENST00000409245.5:c.964-2937_964-2925delinsTGCTGCTGCTGCC	ENSP00000386307.1:n.964-2937_964-2925delinsTGCTGCTGCTGCC
ENST00000409825.5:c.1014-2937_1014-2925delinsTGCTGCTGCTGCC
ENST00000441914.5:c.907-2937_907-2925delinsTGCTGCTGCTGCC
ENST00000461601.5:n.1391-2937_1391-2925delinsTGCTGCTGCTGCC
ENST00000474321.6:n.550-2937_550-2925delinsTGCTGCTGCTGCC
ENST00000484061.5:n.349-2937_349-2925delinsTGCTGCTGCTGCC
ENST00000491786.5:n.470-2937_470-2925delinsTGCTGCTGCTGCC
NM_001288951.1:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC	NP_001275880.1:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
NM_001288953.1:c.964-2937_964-2925delinsTGCTGCTGCTGCC	NP_001275882.1:n.964-2937_964-2925delinsTGCTGCTGCTGCC
NM_001288955.1:c.4-2937_4-2925delinsTGCTGCTGCTGCC	NP_001275884.1:n.4-2937_4-2925delinsTGCTGCTGCTGCC
NM_020458.3:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC	NP_065191.2:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
XM_005264439.2:c.709-2937_709-2925delinsTGCTGCTGCTGCC	XP_005264496.1:n.709-2937_709-2925delinsTGCTGCTGCTGCC
XM_011532998.1:c.709-2937_709-2925delinsTGCTGCTGCTGCC	XP_011531300.1:n.709-2937_709-2925delinsTGCTGCTGCTGCC
XM_011532999.1:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC	XP_011531301.1:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
XM_011533000.1:c.286-2937_286-2925delinsTGCTGCTGCTGCC	XP_011531302.1:n.286-2937_286-2925delinsTGCTGCTGCTGCC
XR_939696.1:n.1371-2937_1371-2925delinsTGCTGCTGCTGCC
XM_005264439.4:c.709-2937_709-2925delinsTGCTGCTGCTGCC	XP_005264496.1:n.709-2937_709-2925delinsTGCTGCTGCTGCC
XM_011532998.3:c.709-2937_709-2925delinsTGCTGCTGCTGCC	XP_011531300.1:n.709-2937_709-2925delinsTGCTGCTGCTGCC
XM_011532999.2:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC	XP_011531301.1:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
XM_011533000.3:c.286-2937_286-2925delinsTGCTGCTGCTGCC	XP_011531302.1:n.286-2937_286-2925delinsTGCTGCTGCTGCC
XM_017004524.1:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC	XP_016860013.1:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
XM_017004525.1:c.898-2937_898-2925delinsTGCTGCTGCTGCC	XP_016860014.1:n.898-2937_898-2925delinsTGCTGCTGCTGCC
XM_017004526.1:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC	XP_016860015.1:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
XM_017004529.1:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC	XP_016860018.1:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
XM_024453013.1:c.31-2937_31-2925delinsTGCTGCTGCTGCC	XP_024308781.1:n.31-2937_31-2925delinsTGCTGCTGCTGCC
XR_001738853.2:n.1378-2937_1378-2925delinsTGCTGCTGCTGCC
XR_001738854.1:n.1377-2937_1377-2925delinsTGCTGCTGCTGCC
NM_020458.4:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC MANE Select	NP_065191.2:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
NM_001288951.2:c.1066-2937_1066-2925delinsTGCTGCTGCTGCC	NP_001275880.1:n.1066-2937_1066-2925delinsTGCTGCTGCTGCC
NM_001288953.2:c.964-2937_964-2925delinsTGCTGCTGCTGCC	NP_001275882.1:n.964-2937_964-2925delinsTGCTGCTGCTGCC
NM_001288955.2:c.4-2937_4-2925delinsTGCTGCTGCTGCC	NP_001275884.1:n.4-2937_4-2925delinsTGCTGCTGCTGCC