Canonical Allele Identifier: CA398388469

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15909811A>T (hg19) ; chr17:g.16006497A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16006497A>T , CM000679.2:g.16006497A>T	GRCh38
NC_000017.10:g.15909811A>T , CM000679.1:g.15909811A>T	GRCh37
NC_000017.9:g.15850536A>T	NCBI36
NG_029806.1:g.12118A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.605A>T MANE Select	ENSP00000261647.5:p.Tyr202Phe
ENST00000261647.9:c.605A>T	ENSP00000261647.5:p.Tyr202Phe
ENST00000475723.5:c.789A>T
ENST00000497842.6:n.715A>T
NM_001271420.1:c.284A>T	NP_001258349.1:p.Tyr95Phe
NM_017775.3:c.605A>T	NP_060245.3:p.Tyr202Phe
XM_011523950.1:c.605A>T	XP_011522252.1:p.Tyr202Phe
XR_934261.1:n.1791+666T>A
XM_017024801.2:c.605A>T	XP_016880290.2:p.Tyr202Phe
XM_017024802.2:c.605A>T	XP_016880291.2:p.Tyr202Phe
XM_024450814.1:c.605A>T	XP_024306582.1:p.Tyr202Phe
NM_017775.4:c.605A>T MANE Select	NP_060245.3:p.Tyr202Phe
NM_001271420.2:c.284A>T	NP_001258349.1:p.Tyr95Phe