Canonical Allele Identifier: CA1030236922

Gene: TTC7A

Linked Data

• dbSNP Id: rs1676903410
• gnomAD v3: 2-47002322-AGAG-A
• gnomAD v4: 2-47002322-AGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47002326_47002328del , CM000664.2:g.47002326_47002328del	GRCh38
NC_000002.11:g.47229465_47229467del , CM000664.1:g.47229465_47229467del	GRCh37
NC_000002.10:g.47082969_47082971del	NCBI36
NG_034143.1:g.91198_91200del
NG_034143.2:g.91198_91200del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698500.1:n.2899-3596_2899-3594del
ENST00000319190.11:c.1066-3596_1066-3594del MANE Select	ENSP00000316699.5:n.1066-3596_1066-3594del
ENST00000319190.9:c.1066-3596_1066-3594del	ENSP00000316699.5:n.1066-3596_1066-3594del
ENST00000394850.6:c.1066-3596_1066-3594del	ENSP00000378320.2:n.1066-3596_1066-3594del
ENST00000409245.5:c.964-3596_964-3594del	ENSP00000386307.1:n.964-3596_964-3594del
ENST00000409825.5:c.1014-3596_1014-3594del
ENST00000441914.5:c.907-3596_907-3594del
ENST00000461601.5:n.1391-3596_1391-3594del
ENST00000474321.6:n.550-3596_550-3594del
ENST00000484061.5:n.349-3596_349-3594del
ENST00000491786.5:n.470-3596_470-3594del
NM_001288951.1:c.1066-3596_1066-3594del	NP_001275880.1:n.1066-3596_1066-3594del
NM_001288953.1:c.964-3596_964-3594del	NP_001275882.1:n.964-3596_964-3594del
NM_001288955.1:c.4-3596_4-3594del	NP_001275884.1:n.4-3596_4-3594del
NM_020458.3:c.1066-3596_1066-3594del	NP_065191.2:n.1066-3596_1066-3594del
XM_005264439.2:c.709-3596_709-3594del	XP_005264496.1:n.709-3596_709-3594del
XM_011532998.1:c.709-3596_709-3594del	XP_011531300.1:n.709-3596_709-3594del
XM_011532999.1:c.1066-3596_1066-3594del	XP_011531301.1:n.1066-3596_1066-3594del
XM_011533000.1:c.286-3596_286-3594del	XP_011531302.1:n.286-3596_286-3594del
XR_939696.1:n.1371-3596_1371-3594del
XM_005264439.4:c.709-3596_709-3594del	XP_005264496.1:n.709-3596_709-3594del
XM_011532998.3:c.709-3596_709-3594del	XP_011531300.1:n.709-3596_709-3594del
XM_011532999.2:c.1066-3596_1066-3594del	XP_011531301.1:n.1066-3596_1066-3594del
XM_011533000.3:c.286-3596_286-3594del	XP_011531302.1:n.286-3596_286-3594del
XM_017004524.1:c.1066-3596_1066-3594del	XP_016860013.1:n.1066-3596_1066-3594del
XM_017004525.1:c.898-3596_898-3594del	XP_016860014.1:n.898-3596_898-3594del
XM_017004526.1:c.1066-3596_1066-3594del	XP_016860015.1:n.1066-3596_1066-3594del
XM_017004529.1:c.1066-3596_1066-3594del	XP_016860018.1:n.1066-3596_1066-3594del
XM_024453013.1:c.30+3447_30+3449del	XP_024308781.1:n.30+3447_30+3449del
XR_001738853.2:n.1378-3596_1378-3594del
XR_001738854.1:n.1377-3596_1377-3594del
NM_020458.4:c.1066-3596_1066-3594del MANE Select	NP_065191.2:n.1066-3596_1066-3594del
NM_001288951.2:c.1066-3596_1066-3594del	NP_001275880.1:n.1066-3596_1066-3594del
NM_001288953.2:c.964-3596_964-3594del	NP_001275882.1:n.964-3596_964-3594del
NM_001288955.2:c.4-3596_4-3594del	NP_001275884.1:n.4-3596_4-3594del