Canonical Allele Identifier: CA2636262702

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028090-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028090G>T , CM000679.2:g.16028090G>T	GRCh38
NC_000017.10:g.15931404G>T , CM000679.1:g.15931404G>T	GRCh37
NC_000017.9:g.15872129G>T	NCBI36
NG_029806.1:g.33711G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*568G>T MANE Select	ENSP00000261647.5:n.*568G>T
ENST00000261647.9:c.*568G>T	ENSP00000261647.5:n.*568G>T
ENST00000465567.1:n.2105G>T
ENST00000470649.1:c.247+1388G>T	ENSP00000465627.1:n.247+1388G>T
ENST00000475723.5:c.1895G>T
ENST00000481107.1:n.2379G>T
NM_001271420.1:c.*568G>T	NP_001258349.1:n.*568G>T
NM_017775.3:c.*568G>T	NP_060245.3:n.*568G>T
XM_017024801.2:c.994+1388G>T	XP_016880290.2:n.994+1388G>T
XM_017024802.2:c.994+1388G>T	XP_016880291.2:n.994+1388G>T
NM_017775.4:c.*568G>T MANE Select	NP_060245.3:n.*568G>T
NM_001271420.2:c.*568G>T	NP_001258349.1:n.*568G>T