Canonical Allele Identifier: CA2636259688

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999911-C-CCGGGGCTGCTCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999914_15999926dup , CM000679.2:g.15999914_15999926dup	GRCh38
NC_000017.10:g.15903228_15903240dup , CM000679.1:g.15903228_15903240dup	GRCh37
NC_000017.9:g.15843953_15843965dup	NCBI36
NG_029806.1:g.5535_5547dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.66_78dup MANE Select	ENSP00000261647.5:p.Arg27GlyfsTer?
ENST00000261647.9:c.66_78dup	ENSP00000261647.5:p.Arg27GlyfsTer?
ENST00000466729.5:c.131_143dup
ENST00000470399.1:c.81_93dup	ENSP00000465082.1:p.Arg32GlyfsTer?
ENST00000475723.5:c.113_125dup
ENST00000497842.6:n.91_103dup
ENST00000583704.1:n.91_103dup
NM_001271420.1:c.-393_-381dup	NP_001258349.1:n.-393_-381dup
NM_017775.3:c.66_78dup	NP_060245.3:p.Arg27GlyfsTer?
XM_011523950.1:c.66_78dup	XP_011522252.1:p.Arg27GlyfsTer?
XM_017024801.2:c.66_78dup	XP_016880290.2:p.Arg27GlyfsTer?
XM_017024802.2:c.66_78dup	XP_016880291.2:p.Arg27GlyfsTer?
XM_024450814.1:c.66_78dup	XP_024306582.1:p.Arg27GlyfsTer?
NM_017775.4:c.66_78dup MANE Select	NP_060245.3:p.Arg27GlyfsTer?
NM_001271420.2:c.-393_-381dup	NP_001258349.1:n.-393_-381dup