Canonical Allele Identifier: CA2563815943

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028223G>A , CM000679.2:g.16028223G>A	GRCh38
NC_000017.10:g.15931537G>A , CM000679.1:g.15931537G>A	GRCh37
NC_000017.9:g.15872262G>A	NCBI36
NG_029806.1:g.33844G>A
NG_047111.1:g.193524C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*701G>A MANE Select	ENSP00000261647.5:n.*701G>A
ENST00000261647.9:c.*701G>A	ENSP00000261647.5:n.*701G>A
ENST00000465567.1:n.2238G>A
ENST00000470649.1:c.247+1521G>A	ENSP00000465627.1:n.247+1521G>A
ENST00000475723.5:c.2028G>A
ENST00000481107.1:n.2512G>A
NM_001271420.1:c.*701G>A	NP_001258349.1:n.*701G>A
NM_017775.3:c.*701G>A	NP_060245.3:n.*701G>A
XM_017024801.2:c.994+1521G>A	XP_016880290.2:n.994+1521G>A
XM_017024802.2:c.994+1521G>A	XP_016880291.2:n.994+1521G>A
NM_017775.4:c.*701G>A MANE Select	NP_060245.3:n.*701G>A
NM_001271420.2:c.*701G>A	NP_001258349.1:n.*701G>A