Canonical Allele Identifier: CA2636262820

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028287-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028289_16028290del , CM000679.2:g.16028289_16028290del	GRCh38
NC_000017.10:g.15931603_15931604del , CM000679.1:g.15931603_15931604del	GRCh37
NC_000017.9:g.15872328_15872329del	NCBI36
NG_029806.1:g.33910_33911del
NG_047111.1:g.193458_193459del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*767_*768del MANE Select	ENSP00000261647.5:n.*767_*768del
ENST00000261647.9:c.*767_*768del	ENSP00000261647.5:n.*767_*768del
ENST00000465567.1:n.2304_2305del
ENST00000470649.1:c.247+1587_247+1588del	ENSP00000465627.1:n.247+1587_247+1588del
ENST00000475723.5:c.2094_2095del
ENST00000481107.1:n.2578_2579del
NM_001271420.1:c.*767_*768del	NP_001258349.1:n.*767_*768del
NM_017775.3:c.*767_*768del	NP_060245.3:n.*767_*768del
XM_017024801.2:c.994+1587_994+1588del	XP_016880290.2:n.994+1587_994+1588del
XM_017024802.2:c.994+1587_994+1588del	XP_016880291.2:n.994+1587_994+1588del
NM_017775.4:c.*767_*768del MANE Select	NP_060245.3:n.*767_*768del
NM_001271420.2:c.*767_*768del	NP_001258349.1:n.*767_*768del