Canonical Allele Identifier: CA358419311

Gene: TTC29

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.146937593C>A , CM000666.2:g.146937593C>A	GRCh38
NC_000004.11:g.147858745C>A , CM000666.1:g.147858745C>A	GRCh37
NC_000004.10:g.148078195C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325106.9:c.176+1G>T MANE Select	ENSP00000316740.4:n.176+1G>T
ENST00000325106.8:c.176+1G>T	ENSP00000316740.4:n.176+1G>T
ENST00000398886.8:c.176+1G>T	ENSP00000381861.5:n.176+1G>T
ENST00000504425.5:c.176+1G>T	ENSP00000425778.1:n.176+1G>T
ENST00000508306.5:c.176+1G>T	ENSP00000422648.1:n.176+1G>T
ENST00000513335.5:c.254+1G>T	ENSP00000423505.1:n.254+1G>T
ENST00000515315.1:c.254+1G>T	ENSP00000423646.1:n.254+1G>T
NM_001300761.1:c.254+1G>T	NP_001287690.1:n.254+1G>T
NM_031956.2:c.176+1G>T	NP_114162.2:n.176+1G>T
XM_005263270.1:c.254+1G>T	XP_005263327.1:n.254+1G>T
XM_006714335.1:c.254+1G>T	XP_006714398.1:n.254+1G>T
XM_006714336.1:c.254+1G>T	XP_006714399.1:n.254+1G>T
XM_006714338.1:c.176+1G>T	XP_006714401.1:n.176+1G>T
XM_006714339.1:c.254+1G>T	XP_006714402.1:n.254+1G>T
XM_011532310.1:c.254+1G>T	XP_011530612.1:n.254+1G>T
XR_427552.1:n.490+1G>T
XR_938777.1:n.490+1G>T
XR_938778.1:n.490+1G>T
XR_938779.1:n.371+1G>T
XR_939304.1:n.331-3062C>A
XR_939305.1:n.331-3062C>A
XR_939306.1:n.331-3062C>A
XR_939307.1:n.330+3256C>A
XR_939308.1:n.331-3062C>A
XR_939309.1:n.330+3256C>A
XR_939310.1:n.331-3062C>A
XR_939311.1:n.331-3062C>A
XR_939312.1:n.331-3062C>A
XR_939313.1:n.331-3062C>A
NM_001300761.2:c.254+1G>T	NP_001287690.1:n.254+1G>T
NM_001317806.1:c.176+1G>T	NP_001304735.1:n.176+1G>T
NM_031956.3:c.176+1G>T	NP_114162.2:n.176+1G>T
NR_133922.1:n.407+1G>T
XM_006714339.2:c.254+1G>T	XP_006714402.1:n.254+1G>T
XM_011532310.2:c.254+1G>T	XP_011530612.1:n.254+1G>T
XM_024454241.1:c.176+1G>T	XP_024310009.1:n.176+1G>T
XR_001741873.2:n.382+3256C>A
XR_001741874.1:n.382+3256C>A
XR_001741875.1:n.382+3256C>A
XR_001741876.1:n.382+3256C>A
XR_001741877.1:n.382+3256C>A
XR_001741878.1:n.382+3256C>A
NM_001300761.3:c.254+1G>T	NP_001287690.1:n.254+1G>T
NM_001317806.2:c.176+1G>T	NP_001304735.1:n.176+1G>T
NR_133922.2:n.385+1G>T
NM_001300761.4:c.254+1G>T	NP_001287690.1:n.254+1G>T
NM_001317806.3:c.176+1G>T	NP_001304735.1:n.176+1G>T
NM_031956.4:c.176+1G>T MANE Select	NP_114162.2:n.176+1G>T
NR_133922.3:n.385+1G>T