Canonical Allele Identifier: CA2830535991

Gene: TTC14

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180605190del , CM000665.2:g.180605190del	GRCh38
NC_000003.11:g.180322978del , CM000665.1:g.180322978del	GRCh37
NC_000003.10:g.181805672del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000296015.9:c.857+183del MANE Select	ENSP00000296015.4:n.857+183del
ENST00000296015.8:c.857+183del	ENSP00000296015.4:n.857+183del
ENST00000382584.8:c.857+183del	ENSP00000372027.4:n.857+183del
ENST00000412756.6:c.857+183del	ENSP00000413743.2:n.857+183del
ENST00000465065.5:c.*1825del	ENSP00000420732.1:n.*1825del
ENST00000470669.5:c.857+183del	ENSP00000419562.1:n.857+183del
ENST00000473854.5:c.354-2199del
NM_001042601.2:c.857+183del	NP_001036066.1:n.857+183del
NM_001288582.1:c.857+183del	NP_001275511.1:n.857+183del
NM_133462.3:c.857+183del	NP_597719.1:n.857+183del
XM_011512439.1:c.107+183del	XP_011510741.1:n.107+183del
XR_427362.2:n.976+183del
XM_017005739.2:c.702-576del	XP_016861228.1:n.702-576del
XM_017005740.2:c.857+183del	XP_016861229.1:n.857+183del
XM_024453361.1:c.107+183del	XP_024309129.1:n.107+183del
XR_001740029.2:n.956+183del
XR_001740030.2:n.956+183del
XR_427362.4:n.956+183del
NM_133462.4:c.857+183del MANE Select	NP_597719.1:n.857+183del
NM_001042601.3:c.857+183del	NP_001036066.1:n.857+183del
NM_001288582.2:c.857+183del	NP_001275511.1:n.857+183del