Canonical Allele Identifier: CA8407627

Gene: TTC19

Linked Data

• dbSNP Id: rs773422746
• ExAC: 17:15930922 TA / T
• gnomAD v2: 17-15930922-TA-T
• gnomAD v4: 17-16027608-TA-T
• MyVariant Identifiers: chr17:g.15930923del (hg19) ; chr17:g.16027609del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027611del , CM000679.2:g.16027611del	GRCh38
NC_000017.10:g.15930925del , CM000679.1:g.15930925del	GRCh37
NC_000017.9:g.15871650del	NCBI36
NG_029806.1:g.33232del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*89del MANE Select	ENSP00000261647.5:n.*89del
ENST00000261647.9:c.*89del	ENSP00000261647.5:n.*89del
ENST00000465567.1:n.1626del
ENST00000470649.1:c.247+909del	ENSP00000465627.1:n.247+909del
ENST00000475723.5:c.1416del
ENST00000481107.1:n.1900del
NM_001271420.1:c.*89del	NP_001258349.1:n.*89del
NM_017775.3:c.*89del	NP_060245.3:n.*89del
XM_017024801.2:c.994+909del	XP_016880290.2:n.994+909del
XM_017024802.2:c.994+909del	XP_016880291.2:n.994+909del
NM_017775.4:c.*89del MANE Select	NP_060245.3:n.*89del
NM_001271420.2:c.*89del	NP_001258349.1:n.*89del