Canonical Allele Identifier: CA726464174

Gene: TTC19

Linked Data

• dbSNP Id: rs1555530900
• MyVariant Identifiers: chr17:g.15931773_15931774insAAAC (hg19) ; chr17:g.16028459_16028460insAAAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028461_16028464dup , CM000679.2:g.16028461_16028464dup	GRCh38
NC_000017.10:g.15931775_15931778dup , CM000679.1:g.15931775_15931778dup	GRCh37
NC_000017.9:g.15872500_15872503dup	NCBI36
NG_029806.1:g.34082_34085dup
NG_047111.1:g.193284_193287dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*939_*942dup MANE Select	ENSP00000261647.5:n.*939_*942dup
ENST00000261647.9:c.*939_*942dup	ENSP00000261647.5:n.*939_*942dup
ENST00000465567.1:n.2476_2479dup
ENST00000470649.1:c.247+1759_247+1762dup	ENSP00000465627.1:n.247+1759_247+1762dup
ENST00000475723.5:c.2266_2269dup
ENST00000481107.1:n.2750_2753dup
NM_001271420.1:c.*939_*942dup	NP_001258349.1:n.*939_*942dup
NM_017775.3:c.*939_*942dup	NP_060245.3:n.*939_*942dup
XM_017024801.2:c.994+1759_994+1762dup	XP_016880290.2:n.994+1759_994+1762dup
XM_017024802.2:c.994+1759_994+1762dup	XP_016880291.2:n.994+1759_994+1762dup
NM_017775.4:c.*939_*942dup MANE Select	NP_060245.3:n.*939_*942dup
NM_001271420.2:c.*939_*942dup	NP_001258349.1:n.*939_*942dup