Canonical Allele Identifier: CA2249869993

Gene: TTC19

Linked Data

• dbSNP Id: rs1971613055

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027583_16027585del , CM000679.2:g.16027583_16027585del	GRCh38
NC_000017.10:g.15930897_15930899del , CM000679.1:g.15930897_15930899del	GRCh37
NC_000017.9:g.15871622_15871624del	NCBI36
NG_029806.1:g.33204_33206del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*61_*63del MANE Select	ENSP00000261647.5:n.*61_*63del
ENST00000261647.9:c.*61_*63del	ENSP00000261647.5:n.*61_*63del
ENST00000465567.1:n.1598_1600del
ENST00000470649.1:c.247+881_247+883del	ENSP00000465627.1:n.247+881_247+883del
ENST00000475723.5:c.1388_1390del
ENST00000481107.1:n.1872_1874del
NM_001271420.1:c.*61_*63del	NP_001258349.1:n.*61_*63del
NM_017775.3:c.*61_*63del	NP_060245.3:n.*61_*63del
XM_017024801.2:c.994+881_994+883del	XP_016880290.2:n.994+881_994+883del
XM_017024802.2:c.994+881_994+883del	XP_016880291.2:n.994+881_994+883del
NM_017775.4:c.*61_*63del MANE Select	NP_060245.3:n.*61_*63del
NM_001271420.2:c.*61_*63del	NP_001258349.1:n.*61_*63del