Canonical Allele Identifier: CA2741521497

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027662G>T , CM000679.2:g.16027662G>T	GRCh38
NC_000017.10:g.15930976G>T , CM000679.1:g.15930976G>T	GRCh37
NC_000017.9:g.15871701G>T	NCBI36
NG_029806.1:g.33283G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*140G>T MANE Select	ENSP00000261647.5:n.*140G>T
ENST00000261647.9:c.*140G>T	ENSP00000261647.5:n.*140G>T
ENST00000465567.1:n.1677G>T
ENST00000470649.1:c.247+960G>T	ENSP00000465627.1:n.247+960G>T
ENST00000475723.5:c.1467G>T
ENST00000481107.1:n.1951G>T
NM_001271420.1:c.*140G>T	NP_001258349.1:n.*140G>T
NM_017775.3:c.*140G>T	NP_060245.3:n.*140G>T
XM_017024801.2:c.994+960G>T	XP_016880290.2:n.994+960G>T
XM_017024802.2:c.994+960G>T	XP_016880291.2:n.994+960G>T
NM_017775.4:c.*140G>T MANE Select	NP_060245.3:n.*140G>T
NM_001271420.2:c.*140G>T	NP_001258349.1:n.*140G>T