Canonical Allele Identifier: CA2636263712

Gene: TTC19

Linked Data

• gnomAD v4: 17-16028818-C-CAAAAAATAAAAAAAAAAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028824_16028825insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000679.2:g.16028824_16028825insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000017.10:g.15932138_15932139insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000679.1:g.15932138_15932139insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000017.9:g.15872863_15872864insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_029806.1:g.34445_34446insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NG_047111.1:g.192928_192929insTTTTTTTTTTTTTTTTTTTTTTATTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select	ENSP00000261647.5:n.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000261647.9:c.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000261647.5:n.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAA...
ENST00000470649.1:c.247+2122_247+2123insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA	ENSP00000465627.1:n.247+2122_247+2123insTAAAAAAAAAAAAAAAAAAAA...
NM_001271420.1:c.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_001258349.1:n.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_017775.3:c.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_060245.3:n.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA
XM_017024801.2:c.994+2122_994+2123insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_016880290.2:n.994+2122_994+2123insTAAAAAAAAAAAAAAAAAAAAAAA...
XM_017024802.2:c.994+2122_994+2123insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XP_016880291.2:n.994+2122_994+2123insTAAAAAAAAAAAAAAAAAAAAAAA...
NM_017775.4:c.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA MANE Select	NP_060245.3:n.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA
NM_001271420.2:c.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NP_001258349.1:n.*1302_*1303insTAAAAAAAAAAAAAAAAAAAAAAAAAAAA