Canonical Allele Identifier: CA2249814982

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999910_15999935delinsGCCGGGGCTGCTCCGCGCGCCTGCTC , CM000679.2:g.15999910_15999935delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	GRCh38
NC_000017.10:g.15903224_15903249delinsGCCGGGGCTGCTCCGCGCGCCTGCTC , CM000679.1:g.15903224_15903249delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	GRCh37
NC_000017.9:g.15843949_15843974delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	NCBI36
NG_029806.1:g.5531_5556delinsGCCGGGGCTGCTCCGCGCGCCTGCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.62_87delinsGCCGGGGCTGCTCCGCGCGCCTGCTC MANE Select	ENSP00000261647.5:p.Cys21=
ENST00000261647.9:c.62_87delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	ENSP00000261647.5:p.Cys21=
ENST00000466729.5:c.127_152delinsGCCGGGGCTGCTCCGCGCGCCTGCTC
ENST00000470399.1:c.77_102delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	ENSP00000465082.1:p.Cys26=
ENST00000475723.5:c.109_134delinsGCCGGGGCTGCTCCGCGCGCCTGCTC
ENST00000497842.6:n.87_112delinsGCCGGGGCTGCTCCGCGCGCCTGCTC
ENST00000583704.1:n.87_112delinsGCCGGGGCTGCTCCGCGCGCCTGCTC
NM_001271420.1:c.-397_-372delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	NP_001258349.1:n.-397_-372delinsGCCGGGGCTGCTCCGCGCGCCTGCTC
NM_017775.3:c.62_87delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	NP_060245.3:p.Cys21=
XM_011523950.1:c.62_87delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	XP_011522252.1:p.Cys21=
XM_017024801.2:c.62_87delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	XP_016880290.2:p.Cys21=
XM_017024802.2:c.62_87delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	XP_016880291.2:p.Cys21=
XM_024450814.1:c.62_87delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	XP_024306582.1:p.Cys21=
NM_017775.4:c.62_87delinsGCCGGGGCTGCTCCGCGCGCCTGCTC MANE Select	NP_060245.3:p.Cys21=
NM_001271420.2:c.-397_-372delinsGCCGGGGCTGCTCCGCGCGCCTGCTC	NP_001258349.1:n.-397_-372delinsGCCGGGGCTGCTCCGCGCGCCTGCTC