Canonical Allele Identifier: CA2636262989

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028659-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028660del , CM000679.2:g.16028660del	GRCh38
NC_000017.10:g.15931974del , CM000679.1:g.15931974del	GRCh37
NC_000017.9:g.15872699del	NCBI36
NG_029806.1:g.34281del
NG_047111.1:g.193087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1138del MANE Select	ENSP00000261647.5:n.*1138del
ENST00000261647.9:c.*1138del	ENSP00000261647.5:n.*1138del
ENST00000465567.1:n.2675del
ENST00000470649.1:c.247+1958del	ENSP00000465627.1:n.247+1958del
ENST00000475723.5:c.2465del
ENST00000481107.1:n.2949del
NM_001271420.1:c.*1138del	NP_001258349.1:n.*1138del
NM_017775.3:c.*1138del	NP_060245.3:n.*1138del
XM_017024801.2:c.994+1958del	XP_016880290.2:n.994+1958del
XM_017024802.2:c.994+1958del	XP_016880291.2:n.994+1958del
NM_017775.4:c.*1138del MANE Select	NP_060245.3:n.*1138del
NM_001271420.2:c.*1138del	NP_001258349.1:n.*1138del