Canonical Allele Identifier: CA46621821

Gene: TTC7A

Linked Data

• dbSNP Id: rs950903252
• MyVariant Identifiers: chr2:g.47229643_47229644del (hg19) ; chr2:g.47002504_47002505del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47002507_47002508del , CM000664.2:g.47002507_47002508del	GRCh38
NC_000002.11:g.47229646_47229647del , CM000664.1:g.47229646_47229647del	GRCh37
NC_000002.10:g.47083150_47083151del	NCBI36
NG_034143.1:g.91379_91380del
NG_034143.2:g.91379_91380del

Transcript Alleles

HGVS	Amino-acid change
ENST00000698500.1:n.2899-3415_2899-3414del
ENST00000319190.11:c.1066-3415_1066-3414del MANE Select	ENSP00000316699.5:n.1066-3415_1066-3414del
ENST00000319190.9:c.1066-3415_1066-3414del	ENSP00000316699.5:n.1066-3415_1066-3414del
ENST00000394850.6:c.1066-3415_1066-3414del	ENSP00000378320.2:n.1066-3415_1066-3414del
ENST00000409245.5:c.964-3415_964-3414del	ENSP00000386307.1:n.964-3415_964-3414del
ENST00000409825.5:c.1014-3415_1014-3414del
ENST00000441914.5:c.907-3415_907-3414del
ENST00000461601.5:n.1391-3415_1391-3414del
ENST00000474321.6:n.550-3415_550-3414del
ENST00000484061.5:n.349-3415_349-3414del
ENST00000491786.5:n.470-3415_470-3414del
NM_001288951.1:c.1066-3415_1066-3414del	NP_001275880.1:n.1066-3415_1066-3414del
NM_001288953.1:c.964-3415_964-3414del	NP_001275882.1:n.964-3415_964-3414del
NM_001288955.1:c.4-3415_4-3414del	NP_001275884.1:n.4-3415_4-3414del
NM_020458.3:c.1066-3415_1066-3414del	NP_065191.2:n.1066-3415_1066-3414del
XM_005264439.2:c.709-3415_709-3414del	XP_005264496.1:n.709-3415_709-3414del
XM_011532998.1:c.709-3415_709-3414del	XP_011531300.1:n.709-3415_709-3414del
XM_011532999.1:c.1066-3415_1066-3414del	XP_011531301.1:n.1066-3415_1066-3414del
XM_011533000.1:c.286-3415_286-3414del	XP_011531302.1:n.286-3415_286-3414del
XR_939696.1:n.1371-3415_1371-3414del
XM_005264439.4:c.709-3415_709-3414del	XP_005264496.1:n.709-3415_709-3414del
XM_011532998.3:c.709-3415_709-3414del	XP_011531300.1:n.709-3415_709-3414del
XM_011532999.2:c.1066-3415_1066-3414del	XP_011531301.1:n.1066-3415_1066-3414del
XM_011533000.3:c.286-3415_286-3414del	XP_011531302.1:n.286-3415_286-3414del
XM_017004524.1:c.1066-3415_1066-3414del	XP_016860013.1:n.1066-3415_1066-3414del
XM_017004525.1:c.898-3415_898-3414del	XP_016860014.1:n.898-3415_898-3414del
XM_017004526.1:c.1066-3415_1066-3414del	XP_016860015.1:n.1066-3415_1066-3414del
XM_017004529.1:c.1066-3415_1066-3414del	XP_016860018.1:n.1066-3415_1066-3414del
XM_024453013.1:c.31-3415_31-3414del	XP_024308781.1:n.31-3415_31-3414del
XR_001738853.2:n.1378-3415_1378-3414del
XR_001738854.1:n.1377-3415_1377-3414del
NM_020458.4:c.1066-3415_1066-3414del MANE Select	NP_065191.2:n.1066-3415_1066-3414del
NM_001288951.2:c.1066-3415_1066-3414del	NP_001275880.1:n.1066-3415_1066-3414del
NM_001288953.2:c.964-3415_964-3414del	NP_001275882.1:n.964-3415_964-3414del
NM_001288955.2:c.4-3415_4-3414del	NP_001275884.1:n.4-3415_4-3414del