Canonical Allele Identifier: CA913203465

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000001_16000004del , CM000679.2:g.16000001_16000004del	GRCh38
NC_000017.10:g.15903315_15903318del , CM000679.1:g.15903315_15903318del	GRCh37
NC_000017.9:g.15844040_15844043del	NCBI36
NG_029806.1:g.5622_5625del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.153_156del MANE Select	ENSP00000261647.5:p.Arg52AlafsTer?
ENST00000261647.9:c.153_156del	ENSP00000261647.5:p.Arg52AlafsTer?
ENST00000466729.5:c.218_221del
ENST00000470399.1:c.168_171del	ENSP00000465082.1:p.Arg57AlafsTer?
ENST00000475723.5:c.200_203del
ENST00000497842.6:n.178_181del
ENST00000583704.1:n.178_181del
NM_001271420.1:c.-306_-303del	NP_001258349.1:n.-306_-303del
NM_017775.3:c.153_156del	NP_060245.3:p.Arg52AlafsTer?
XM_011523950.1:c.153_156del	XP_011522252.1:p.Arg52AlafsTer?
XM_017024801.2:c.153_156del	XP_016880290.2:p.Arg52AlafsTer?
XM_017024802.2:c.153_156del	XP_016880291.2:p.Arg52AlafsTer?
XM_024450814.1:c.153_156del	XP_024306582.1:p.Arg52AlafsTer?
NM_017775.4:c.153_156del MANE Select	NP_060245.3:p.Arg52AlafsTer?
NM_001271420.2:c.-306_-303del	NP_001258349.1:n.-306_-303del