Canonical Allele Identifier: CA2576180960

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999841G>C , CM000679.2:g.15999841G>C	GRCh38
NC_000017.10:g.15903155G>C , CM000679.1:g.15903155G>C	GRCh37
NC_000017.9:g.15843880G>C	NCBI36
NG_029806.1:g.5462G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.-8G>C MANE Select	ENSP00000261647.5:n.-8G>C
ENST00000261647.9:c.-8G>C	ENSP00000261647.5:n.-8G>C
ENST00000466729.5:c.58G>C
ENST00000470399.1:c.8G>C	ENSP00000465082.1:p.Gly3Ala
ENST00000475723.5:c.40G>C
ENST00000497842.6:n.18G>C
ENST00000583704.1:n.18G>C
NM_001271420.1:c.-466G>C	NP_001258349.1:n.-466G>C
NM_017775.3:c.-8G>C	NP_060245.3:n.-8G>C
XM_011523950.1:c.-8G>C	XP_011522252.1:n.-8G>C
XM_017024801.2:c.-8G>C	XP_016880290.2:n.-8G>C
XM_017024802.2:c.-8G>C	XP_016880291.2:n.-8G>C
XM_024450814.1:c.-8G>C	XP_024306582.1:n.-8G>C
NM_017775.4:c.-8G>C MANE Select	NP_060245.3:n.-8G>C
NM_001271420.2:c.-466G>C	NP_001258349.1:n.-466G>C