Canonical Allele Identifier: CA1030237060

Gene: TTC7A

Linked Data

• gnomAD v3: 2-47002527-C-CCG
• gnomAD v4: 2-47002527-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47002527_47002528insCG , CM000664.2:g.47002527_47002528insCG	GRCh38
NC_000002.11:g.47229666_47229667insCG , CM000664.1:g.47229666_47229667insCG	GRCh37
NC_000002.10:g.47083170_47083171insCG	NCBI36
NG_034143.1:g.91399_91400insCG
NG_034143.2:g.91399_91400insCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000698500.1:n.2899-3395_2899-3394insCG
ENST00000319190.11:c.1066-3395_1066-3394insCG MANE Select	ENSP00000316699.5:n.1066-3395_1066-3394insCG
ENST00000319190.9:c.1066-3395_1066-3394insCG	ENSP00000316699.5:n.1066-3395_1066-3394insCG
ENST00000394850.6:c.1066-3395_1066-3394insCG	ENSP00000378320.2:n.1066-3395_1066-3394insCG
ENST00000409245.5:c.964-3395_964-3394insCG	ENSP00000386307.1:n.964-3395_964-3394insCG
ENST00000409825.5:c.1014-3395_1014-3394insCG
ENST00000441914.5:c.907-3395_907-3394insCG
ENST00000461601.5:n.1391-3395_1391-3394insCG
ENST00000474321.6:n.550-3395_550-3394insCG
ENST00000484061.5:n.349-3395_349-3394insCG
ENST00000491786.5:n.470-3395_470-3394insCG
NM_001288951.1:c.1066-3395_1066-3394insCG	NP_001275880.1:n.1066-3395_1066-3394insCG
NM_001288953.1:c.964-3395_964-3394insCG	NP_001275882.1:n.964-3395_964-3394insCG
NM_001288955.1:c.4-3395_4-3394insCG	NP_001275884.1:n.4-3395_4-3394insCG
NM_020458.3:c.1066-3395_1066-3394insCG	NP_065191.2:n.1066-3395_1066-3394insCG
XM_005264439.2:c.709-3395_709-3394insCG	XP_005264496.1:n.709-3395_709-3394insCG
XM_011532998.1:c.709-3395_709-3394insCG	XP_011531300.1:n.709-3395_709-3394insCG
XM_011532999.1:c.1066-3395_1066-3394insCG	XP_011531301.1:n.1066-3395_1066-3394insCG
XM_011533000.1:c.286-3395_286-3394insCG	XP_011531302.1:n.286-3395_286-3394insCG
XR_939696.1:n.1371-3395_1371-3394insCG
XM_005264439.4:c.709-3395_709-3394insCG	XP_005264496.1:n.709-3395_709-3394insCG
XM_011532998.3:c.709-3395_709-3394insCG	XP_011531300.1:n.709-3395_709-3394insCG
XM_011532999.2:c.1066-3395_1066-3394insCG	XP_011531301.1:n.1066-3395_1066-3394insCG
XM_011533000.3:c.286-3395_286-3394insCG	XP_011531302.1:n.286-3395_286-3394insCG
XM_017004524.1:c.1066-3395_1066-3394insCG	XP_016860013.1:n.1066-3395_1066-3394insCG
XM_017004525.1:c.898-3395_898-3394insCG	XP_016860014.1:n.898-3395_898-3394insCG
XM_017004526.1:c.1066-3395_1066-3394insCG	XP_016860015.1:n.1066-3395_1066-3394insCG
XM_017004529.1:c.1066-3395_1066-3394insCG	XP_016860018.1:n.1066-3395_1066-3394insCG
XM_024453013.1:c.31-3395_31-3394insCG	XP_024308781.1:n.31-3395_31-3394insCG
XR_001738853.2:n.1378-3395_1378-3394insCG
XR_001738854.1:n.1377-3395_1377-3394insCG
NM_020458.4:c.1066-3395_1066-3394insCG MANE Select	NP_065191.2:n.1066-3395_1066-3394insCG
NM_001288951.2:c.1066-3395_1066-3394insCG	NP_001275880.1:n.1066-3395_1066-3394insCG
NM_001288953.2:c.964-3395_964-3394insCG	NP_001275882.1:n.964-3395_964-3394insCG
NM_001288955.2:c.4-3395_4-3394insCG	NP_001275884.1:n.4-3395_4-3394insCG