Canonical Allele Identifier: CA2249870087

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027660_16027661delinsAG , CM000679.2:g.16027660_16027661delinsAG	GRCh38
NC_000017.10:g.15930974_15930975delinsAG , CM000679.1:g.15930974_15930975delinsAG	GRCh37
NC_000017.9:g.15871699_15871700delinsAG	NCBI36
NG_029806.1:g.33281_33282delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*138_*139delinsAG MANE Select	ENSP00000261647.5:n.*138_*139delinsAG
ENST00000261647.9:c.*138_*139delinsAG	ENSP00000261647.5:n.*138_*139delinsAG
ENST00000465567.1:n.1675_1676delinsAG
ENST00000470649.1:c.247+958_247+959delinsAG	ENSP00000465627.1:n.247+958_247+959delinsAG
ENST00000475723.5:c.1465_1466delinsAG
ENST00000481107.1:n.1949_1950delinsAG
NM_001271420.1:c.*138_*139delinsAG	NP_001258349.1:n.*138_*139delinsAG
NM_017775.3:c.*138_*139delinsAG	NP_060245.3:n.*138_*139delinsAG
XM_017024801.2:c.994+958_994+959delinsAG	XP_016880290.2:n.994+958_994+959delinsAG
XM_017024802.2:c.994+958_994+959delinsAG	XP_016880291.2:n.994+958_994+959delinsAG
NM_017775.4:c.*138_*139delinsAG MANE Select	NP_060245.3:n.*138_*139delinsAG
NM_001271420.2:c.*138_*139delinsAG	NP_001258349.1:n.*138_*139delinsAG