Canonical Allele Identifier: CA2249870808

Gene: TTC19

Linked Data

• dbSNP Id: rs1971648226
• gnomAD v4: 17-16028229-TCTGAACA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028232_16028238del , CM000679.2:g.16028232_16028238del	GRCh38
NC_000017.10:g.15931546_15931552del , CM000679.1:g.15931546_15931552del	GRCh37
NC_000017.9:g.15872271_15872277del	NCBI36
NG_029806.1:g.33853_33859del
NG_047111.1:g.193511_193517del

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*710_*716del MANE Select	ENSP00000261647.5:n.*710_*716del
ENST00000261647.9:c.*710_*716del	ENSP00000261647.5:n.*710_*716del
ENST00000465567.1:n.2247_2253del
ENST00000470649.1:c.247+1530_247+1536del	ENSP00000465627.1:n.247+1530_247+1536del
ENST00000475723.5:c.2037_2043del
ENST00000481107.1:n.2521_2527del
NM_001271420.1:c.*710_*716del	NP_001258349.1:n.*710_*716del
NM_017775.3:c.*710_*716del	NP_060245.3:n.*710_*716del
XM_017024801.2:c.994+1530_994+1536del	XP_016880290.2:n.994+1530_994+1536del
XM_017024802.2:c.994+1530_994+1536del	XP_016880291.2:n.994+1530_994+1536del
NM_017775.4:c.*710_*716del MANE Select	NP_060245.3:n.*710_*716del
NM_001271420.2:c.*710_*716del	NP_001258349.1:n.*710_*716del