Canonical Allele Identifier: CA981831975

Gene: TTC19

Linked Data

• gnomAD v3: 17-16028431-A-ATTTTTT
• gnomAD v4: 17-16028431-A-ATTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028434_16028435insTTTTTT , CM000679.2:g.16028434_16028435insTTTTTT	GRCh38
NC_000017.10:g.15931748_15931749insTTTTTT , CM000679.1:g.15931748_15931749insTTTTTT	GRCh37
NC_000017.9:g.15872473_15872474insTTTTTT	NCBI36
NG_029806.1:g.34055_34056insTTTTTT
NG_047111.1:g.193315_193316insAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*912_*913insTTTTTT MANE Select	ENSP00000261647.5:n.*912_*913insTTTTTT
ENST00000261647.9:c.*912_*913insTTTTTT	ENSP00000261647.5:n.*912_*913insTTTTTT
ENST00000465567.1:n.2449_2450insTTTTTT
ENST00000470649.1:c.247+1732_247+1733insTTTTTT	ENSP00000465627.1:n.247+1732_247+1733insTTTTTT
ENST00000475723.5:c.2239_2240insTTTTTT
ENST00000481107.1:n.2723_2724insTTTTTT
NM_001271420.1:c.*912_*913insTTTTTT	NP_001258349.1:n.*912_*913insTTTTTT
NM_017775.3:c.*912_*913insTTTTTT	NP_060245.3:n.*912_*913insTTTTTT
XM_017024801.2:c.994+1732_994+1733insTTTTTT	XP_016880290.2:n.994+1732_994+1733insTTTTTT
XM_017024802.2:c.994+1732_994+1733insTTTTTT	XP_016880291.2:n.994+1732_994+1733insTTTTTT
NM_017775.4:c.*912_*913insTTTTTT MANE Select	NP_060245.3:n.*912_*913insTTTTTT
NM_001271420.2:c.*912_*913insTTTTTT	NP_001258349.1:n.*912_*913insTTTTTT