Canonical Allele Identifier: CA726464416

Gene: TTC19

Linked Data

• dbSNP Id: rs1232541239
• MyVariant Identifiers: chr17:g.15932069_15932070insCC (hg19) ; chr17:g.16028755_16028756insCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028755_16028756insCC , CM000679.2:g.16028755_16028756insCC	GRCh38
NC_000017.10:g.15932069_15932070insCC , CM000679.1:g.15932069_15932070insCC	GRCh37
NC_000017.9:g.15872794_15872795insCC	NCBI36
NG_029806.1:g.34376_34377insCC
NG_047111.1:g.192991_192992insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*1233_*1234insCC MANE Select	ENSP00000261647.5:n.*1233_*1234insCC
ENST00000261647.9:c.*1233_*1234insCC	ENSP00000261647.5:n.*1233_*1234insCC
ENST00000465567.1:n.2770_2771insCC
ENST00000470649.1:c.247+2053_247+2054insCC	ENSP00000465627.1:n.247+2053_247+2054insCC
ENST00000475723.5:c.2560_2561insCC
ENST00000481107.1:n.3044_3045insCC
NM_001271420.1:c.*1233_*1234insCC	NP_001258349.1:n.*1233_*1234insCC
NM_017775.3:c.*1233_*1234insCC	NP_060245.3:n.*1233_*1234insCC
XM_017024801.2:c.994+2053_994+2054insCC	XP_016880290.2:n.994+2053_994+2054insCC
XM_017024802.2:c.994+2053_994+2054insCC	XP_016880291.2:n.994+2053_994+2054insCC
NM_017775.4:c.*1233_*1234insCC MANE Select	NP_060245.3:n.*1233_*1234insCC
NM_001271420.2:c.*1233_*1234insCC	NP_001258349.1:n.*1233_*1234insCC