Canonical Allele Identifier: CA2808602891

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999955_15999956insT , CM000679.2:g.15999955_15999956insT	GRCh38
NC_000017.10:g.15903269_15903270insT , CM000679.1:g.15903269_15903270insT	GRCh37
NC_000017.9:g.15843994_15843995insT	NCBI36
NG_029806.1:g.5576_5577insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.107_108insT MANE Select	ENSP00000261647.5:p.Pro38AlafsTer?
ENST00000261647.9:c.107_108insT	ENSP00000261647.5:p.Pro38AlafsTer?
ENST00000466729.5:c.172_173insT
ENST00000470399.1:c.122_123insT	ENSP00000465082.1:p.Pro43AlafsTer?
ENST00000475723.5:c.154_155insT
ENST00000497842.6:n.132_133insT
ENST00000583704.1:n.132_133insT
NM_001271420.1:c.-352_-351insT	NP_001258349.1:n.-352_-351insT
NM_017775.3:c.107_108insT	NP_060245.3:p.Pro38AlafsTer?
XM_011523950.1:c.107_108insT	XP_011522252.1:p.Pro38AlafsTer?
XM_017024801.2:c.107_108insT	XP_016880290.2:p.Pro38AlafsTer?
XM_017024802.2:c.107_108insT	XP_016880291.2:p.Pro38AlafsTer?
XM_024450814.1:c.107_108insT	XP_024306582.1:p.Pro38AlafsTer?
NM_017775.4:c.107_108insT MANE Select	NP_060245.3:p.Pro38AlafsTer?
NM_001271420.2:c.-352_-351insT	NP_001258349.1:n.-352_-351insT