Canonical Allele Identifier: CA624957634

Gene: TTC19

Linked Data

• dbSNP Id: rs1567589882
• gnomAD v2: 17-15931824-CTT-C
• gnomAD v4: 17-16028510-CTT-C
• MyVariant Identifiers: chr17:g.15931825_15931826del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028512_16028513del , CM000679.2:g.16028512_16028513del	GRCh38
NC_000017.10:g.15931826_15931827del , CM000679.1:g.15931826_15931827del	GRCh37
NC_000017.9:g.15872551_15872552del	NCBI36
NG_029806.1:g.34133_34134del
NG_047111.1:g.193235_193236del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*990_*991del MANE Select	ENSP00000261647.5:n.*990_*991del
ENST00000261647.9:c.*990_*991del	ENSP00000261647.5:n.*990_*991del
ENST00000465567.1:n.2527_2528del
ENST00000470649.1:c.247+1810_247+1811del	ENSP00000465627.1:n.247+1810_247+1811del
ENST00000475723.5:c.2317_2318del
ENST00000481107.1:n.2801_2802del
NM_001271420.1:c.*990_*991del	NP_001258349.1:n.*990_*991del
NM_017775.3:c.*990_*991del	NP_060245.3:n.*990_*991del
XM_017024801.2:c.994+1810_994+1811del	XP_016880290.2:n.994+1810_994+1811del
XM_017024802.2:c.994+1810_994+1811del	XP_016880291.2:n.994+1810_994+1811del
NM_017775.4:c.*990_*991del MANE Select	NP_060245.3:n.*990_*991del
NM_001271420.2:c.*990_*991del	NP_001258349.1:n.*990_*991del