Canonical Allele Identifier: CA2636262881

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028414-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028414G>T , CM000679.2:g.16028414G>T	GRCh38
NC_000017.10:g.15931728G>T , CM000679.1:g.15931728G>T	GRCh37
NC_000017.9:g.15872453G>T	NCBI36
NG_029806.1:g.34035G>T
NG_047111.1:g.193333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*892G>T MANE Select	ENSP00000261647.5:n.*892G>T
ENST00000261647.9:c.*892G>T	ENSP00000261647.5:n.*892G>T
ENST00000465567.1:n.2429G>T
ENST00000470649.1:c.247+1712G>T	ENSP00000465627.1:n.247+1712G>T
ENST00000475723.5:c.2219G>T
ENST00000481107.1:n.2703G>T
NM_001271420.1:c.*892G>T	NP_001258349.1:n.*892G>T
NM_017775.3:c.*892G>T	NP_060245.3:n.*892G>T
XM_017024801.2:c.994+1712G>T	XP_016880290.2:n.994+1712G>T
XM_017024802.2:c.994+1712G>T	XP_016880291.2:n.994+1712G>T
NM_017775.4:c.*892G>T MANE Select	NP_060245.3:n.*892G>T
NM_001271420.2:c.*892G>T	NP_001258349.1:n.*892G>T