Canonical Allele Identifier: CA2551064183

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028510_16028516del , CM000679.2:g.16028510_16028516del	GRCh38
NC_000017.10:g.15931824_15931830del , CM000679.1:g.15931824_15931830del	GRCh37
NC_000017.9:g.15872549_15872555del	NCBI36
NG_029806.1:g.34131_34137del
NG_047111.1:g.193232_193238del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*988_*994del MANE Select	ENSP00000261647.5:n.*988_*994del
ENST00000261647.9:c.*988_*994del	ENSP00000261647.5:n.*988_*994del
ENST00000465567.1:n.2525_2531del
ENST00000470649.1:c.247+1808_247+1814del	ENSP00000465627.1:n.247+1808_247+1814del
ENST00000475723.5:c.2315_2321del
ENST00000481107.1:n.2799_2805del
NM_001271420.1:c.*988_*994del	NP_001258349.1:n.*988_*994del
NM_017775.3:c.*988_*994del	NP_060245.3:n.*988_*994del
XM_017024801.2:c.994+1808_994+1814del	XP_016880290.2:n.994+1808_994+1814del
XM_017024802.2:c.994+1808_994+1814del	XP_016880291.2:n.994+1808_994+1814del
NM_017775.4:c.*988_*994del MANE Select	NP_060245.3:n.*988_*994del
NM_001271420.2:c.*988_*994del	NP_001258349.1:n.*988_*994del