Canonical Allele Identifier: CA2636259690

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999937-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999941del , CM000679.2:g.15999941del	GRCh38
NC_000017.10:g.15903255del , CM000679.1:g.15903255del	GRCh37
NC_000017.9:g.15843980del	NCBI36
NG_029806.1:g.5562del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.93del MANE Select	ENSP00000261647.5:p.Leu32TrpfsTer?
ENST00000261647.9:c.93del	ENSP00000261647.5:p.Leu32TrpfsTer?
ENST00000466729.5:c.158del
ENST00000470399.1:c.108del	ENSP00000465082.1:p.Leu37TrpfsTer?
ENST00000475723.5:c.140del
ENST00000497842.6:n.118del
ENST00000583704.1:n.118del
NM_001271420.1:c.-366del	NP_001258349.1:n.-366del
NM_017775.3:c.93del	NP_060245.3:p.Leu32TrpfsTer?
XM_011523950.1:c.93del	XP_011522252.1:p.Leu32TrpfsTer?
XM_017024801.2:c.93del	XP_016880290.2:p.Leu32TrpfsTer?
XM_017024802.2:c.93del	XP_016880291.2:p.Leu32TrpfsTer?
XM_024450814.1:c.93del	XP_024306582.1:p.Leu32TrpfsTer?
NM_017775.4:c.93del MANE Select	NP_060245.3:p.Leu32TrpfsTer?
NM_001271420.2:c.-366del	NP_001258349.1:n.-366del