Canonical Allele Identifier: CA441754609

Gene: TTC29

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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