Canonical Allele Identifier: CA2636259682

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999845-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999845G>T , CM000679.2:g.15999845G>T	GRCh38
NC_000017.10:g.15903159G>T , CM000679.1:g.15903159G>T	GRCh37
NC_000017.9:g.15843884G>T	NCBI36
NG_029806.1:g.5466G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.-4G>T MANE Select	ENSP00000261647.5:n.-4G>T
ENST00000261647.9:c.-4G>T	ENSP00000261647.5:n.-4G>T
ENST00000466729.5:c.62G>T
ENST00000470399.1:c.12G>T	ENSP00000465082.1:p.Gly4=
ENST00000475723.5:c.44G>T
ENST00000497842.6:n.22G>T
ENST00000583704.1:n.22G>T
NM_001271420.1:c.-462G>T	NP_001258349.1:n.-462G>T
NM_017775.3:c.-4G>T	NP_060245.3:n.-4G>T
XM_011523950.1:c.-4G>T	XP_011522252.1:n.-4G>T
XM_017024801.2:c.-4G>T	XP_016880290.2:n.-4G>T
XM_017024802.2:c.-4G>T	XP_016880291.2:n.-4G>T
XM_024450814.1:c.-4G>T	XP_024306582.1:n.-4G>T
NM_017775.4:c.-4G>T MANE Select	NP_060245.3:n.-4G>T
NM_001271420.2:c.-462G>T	NP_001258349.1:n.-462G>T