Canonical Allele Identifier: CA8407671

Gene: TTC19

Linked Data

• dbSNP Id: rs760179542
• ExAC: 17:15931508 A / ATTT
• gnomAD v2: 17-15931508-A-ATTT
• gnomAD v3: 17-16028194-A-ATTT
• gnomAD v4: 17-16028194-A-ATTT
• MyVariant Identifiers: chr17:g.15931508_15931509insTTT (hg19) ; chr17:g.16028194_16028195insTTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028194_16028195insTTT , CM000679.2:g.16028194_16028195insTTT	GRCh38
NC_000017.10:g.15931508_15931509insTTT , CM000679.1:g.15931508_15931509insTTT	GRCh37
NC_000017.9:g.15872233_15872234insTTT	NCBI36
NG_029806.1:g.33815_33816insTTT
NG_047111.1:g.193552_193553insAAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*672_*673insTTT MANE Select	ENSP00000261647.5:n.*672_*673insTTT
ENST00000261647.9:c.*672_*673insTTT	ENSP00000261647.5:n.*672_*673insTTT
ENST00000465567.1:n.2209_2210insTTT
ENST00000470649.1:c.247+1492_247+1493insTTT	ENSP00000465627.1:n.247+1492_247+1493insT...
ENST00000475723.5:c.1999_2000insTTT
ENST00000481107.1:n.2483_2484insTTT
NM_001271420.1:c.*672_*673insTTT	NP_001258349.1:n.*672_*673insTTT
NM_017775.3:c.*672_*673insTTT	NP_060245.3:n.*672_*673insTTT
XM_017024801.2:c.994+1492_994+1493insTTT	XP_016880290.2:n.994+1492_994+1493insTTT
XM_017024802.2:c.994+1492_994+1493insTTT	XP_016880291.2:n.994+1492_994+1493insTTT
NM_017775.4:c.*672_*673insTTT MANE Select	NP_060245.3:n.*672_*673insTTT
NM_001271420.2:c.*672_*673insTTT	NP_001258349.1:n.*672_*673insTTT