Canonical Allele Identifier: CA624957601

Gene: TTC19

Linked Data

• dbSNP Id: rs1332704917
• gnomAD v2: 17-15931694-T-TA
• gnomAD v3: 17-16028380-T-TA
• gnomAD v4: 17-16028380-T-TA
• MyVariant Identifiers: chr17:g.15931694_15931695insA (hg19) ; chr17:g.16028380_16028381insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028381dup , CM000679.2:g.16028381dup	GRCh38
NC_000017.10:g.15931695dup , CM000679.1:g.15931695dup	GRCh37
NC_000017.9:g.15872420dup	NCBI36
NG_029806.1:g.34002dup
NG_047111.1:g.193366dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*859dup MANE Select	ENSP00000261647.5:n.*859dup
ENST00000261647.9:c.*859dup	ENSP00000261647.5:n.*859dup
ENST00000465567.1:n.2396dup
ENST00000470649.1:c.247+1679dup	ENSP00000465627.1:n.247+1679dup
ENST00000475723.5:c.2186dup
ENST00000481107.1:n.2670dup
NM_001271420.1:c.*859dup	NP_001258349.1:n.*859dup
NM_017775.3:c.*859dup	NP_060245.3:n.*859dup
XM_017024801.2:c.994+1679dup	XP_016880290.2:n.994+1679dup
XM_017024802.2:c.994+1679dup	XP_016880291.2:n.994+1679dup
NM_017775.4:c.*859dup MANE Select	NP_060245.3:n.*859dup
NM_001271420.2:c.*859dup	NP_001258349.1:n.*859dup