Canonical Allele Identifier: CA10644915

Gene: TTC19

Linked Data

• ClinVar Variation Id: 321959
• ClinVar RCV Id: RCV000369835
• dbSNP Id: rs764835326
• MyVariant Identifiers: chr17:g.15931506dupT (hg19) ; chr17:g.15931505_15931506insT (hg19) ; chr17:g.16028192dupT (hg38) ; chr17:g.16028191_16028192insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028192dup , CM000679.2:g.16028192dup	GRCh38
NC_000017.10:g.15931506dup , CM000679.1:g.15931506dup	GRCh37
NC_000017.9:g.15872231dup	NCBI36
NG_029806.1:g.33813dup
NG_047111.1:g.193555dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*670dup MANE Select	ENSP00000261647.5:n.*670dup
ENST00000261647.9:c.*670dup	ENSP00000261647.5:n.*670dup
ENST00000465567.1:n.2207dup
ENST00000470649.1:c.247+1490dup	ENSP00000465627.1:n.247+1490dup
ENST00000475723.5:c.1997dup
ENST00000481107.1:n.2481dup
NM_001271420.1:c.*670dup	NP_001258349.1:n.*670dup
NM_017775.3:c.*670dup	NP_060245.3:n.*670dup
XM_017024801.2:c.994+1490dup	XP_016880290.2:n.994+1490dup
XM_017024802.2:c.994+1490dup	XP_016880291.2:n.994+1490dup
NM_017775.4:c.*670dup MANE Select	NP_060245.3:n.*670dup
NM_001271420.2:c.*670dup	NP_001258349.1:n.*670dup