Canonical Allele Identifier: CA1501785779

Gene: TTC29

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.146803680G= , CM000666.2:g.146803680G=	GRCh38
NC_000004.11:g.147724832G= , CM000666.1:g.147724832G=	GRCh37
NC_000004.10:g.147944282G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325106.9:c.1107C= MANE Select	ENSP00000316740.4:p.Tyr369=
ENST00000325106.8:c.1107C=	ENSP00000316740.4:p.Tyr369=
ENST00000398886.8:c.*146C=	ENSP00000381861.5:n.*146C=
ENST00000504425.5:c.1107C=	ENSP00000425778.1:p.Tyr369=
ENST00000506019.1:n.280C=
ENST00000508306.5:c.*169C=	ENSP00000422648.1:n.*169C=
ENST00000513335.5:c.1185C=	ENSP00000423505.1:p.Tyr395=
NM_001300761.1:c.1185C=	NP_001287690.1:p.Tyr395=
NM_031956.2:c.1107C=	NP_114162.2:p.Tyr369=
XM_005263270.1:c.1185C=	XP_005263327.1:p.Tyr395=
XM_006714335.1:c.1185C=	XP_006714398.1:p.Tyr395=
XM_006714336.1:c.1185C=	XP_006714399.1:p.Tyr395=
XM_006714338.1:c.1107C=	XP_006714401.1:p.Tyr369=
XM_006714339.1:c.999C=	XP_006714402.1:p.Tyr333=
XR_427552.1:n.1421C=
XR_938777.1:n.1421C=
XR_938778.1:n.1575C=
XR_938779.1:n.1456C=
NM_001300761.2:c.1185C=	NP_001287690.1:p.Tyr395=
NM_001317806.1:c.1107C=	NP_001304735.1:p.Tyr369=
NM_031956.3:c.1107C=	NP_114162.2:p.Tyr369=
NR_133922.1:n.1492C=
XM_006714339.2:c.999C=	XP_006714402.1:p.Tyr333=
XM_024454241.1:c.921C=	XP_024310009.1:p.Tyr307=
NM_001300761.3:c.1185C=	NP_001287690.1:p.Tyr395=
NM_001317806.2:c.1107C=	NP_001304735.1:p.Tyr369=
NR_133922.2:n.1470C=
NM_001300761.4:c.1185C=	NP_001287690.1:p.Tyr395=
NM_001317806.3:c.1107C=	NP_001304735.1:p.Tyr369=
NM_031956.4:c.1107C= MANE Select	NP_114162.2:p.Tyr369=
NR_133922.3:n.1470C=