Canonical Allele Identifier: CA981833008

Gene: TTC19

Linked Data

• gnomAD v3: 17-16028848-T-TAAAAAAAAAA
• gnomAD v4: 17-16028848-T-TAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028848_16028849insAAAAAAAAAA , CM000679.2:g.16028848_16028849insAAAAAAAAAA	GRCh38
NC_000017.10:g.15932162_15932163insAAAAAAAAAA , CM000679.1:g.15932162_15932163insAAAAAAAAAA	GRCh37
NC_000017.9:g.15872887_15872888insAAAAAAAAAA	NCBI36
NG_029806.1:g.34469_34470insAAAAAAAAAA
NG_047111.1:g.192898_192899insTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1326_*1327insAAAAAAAAAA MANE Select	ENSP00000261647.5:n.*1326_*1327insAAAAAAAAAA
ENST00000261647.9:c.*1326_*1327insAAAAAAAAAA	ENSP00000261647.5:n.*1326_*1327insAAAAAAAAAA
ENST00000470649.1:c.247+2146_247+2147insAAAAAAAAAA	ENSP00000465627.1:n.247+2146_247+2147insAAAAAAAAAA
NM_001271420.1:c.*1326_*1327insAAAAAAAAAA	NP_001258349.1:n.*1326_*1327insAAAAAAAAAA
NM_017775.3:c.*1326_*1327insAAAAAAAAAA	NP_060245.3:n.*1326_*1327insAAAAAAAAAA
XM_017024801.2:c.994+2146_994+2147insAAAAAAAAAA	XP_016880290.2:n.994+2146_994+2147insAAAAAAAAAA
XM_017024802.2:c.994+2146_994+2147insAAAAAAAAAA	XP_016880291.2:n.994+2146_994+2147insAAAAAAAAAA
NM_017775.4:c.*1326_*1327insAAAAAAAAAA MANE Select	NP_060245.3:n.*1326_*1327insAAAAAAAAAA
NM_001271420.2:c.*1326_*1327insAAAAAAAAAA	NP_001258349.1:n.*1326_*1327insAAAAAAAAAA