Canonical Allele Identifier: CA398379544

Gene: TTC19

Linked Data

• MyVariant Identifiers: chr17:g.15930819A>T (hg19) ; chr17:g.16027505A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027505A>T , CM000679.2:g.16027505A>T	GRCh38
NC_000017.10:g.15930819A>T , CM000679.1:g.15930819A>T	GRCh37
NC_000017.9:g.15871544A>T	NCBI36
NG_029806.1:g.33126A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1126A>T MANE Select	ENSP00000261647.5:p.Asn376Tyr
ENST00000261647.9:c.1126A>T	ENSP00000261647.5:p.Asn376Tyr
ENST00000465567.1:n.1520A>T
ENST00000470649.1:c.247+803A>T	ENSP00000465627.1:n.247+803A>T
ENST00000475723.5:c.1310A>T
ENST00000481107.1:n.1794A>T
ENST00000497842.6:n.1330A>T
NM_001271420.1:c.805A>T	NP_001258349.1:p.Asn269Tyr
NM_017775.3:c.1126A>T	NP_060245.3:p.Asn376Tyr
XM_017024801.2:c.994+803A>T	XP_016880290.2:n.994+803A>T
XM_017024802.2:c.994+803A>T	XP_016880291.2:n.994+803A>T
NM_017775.4:c.1126A>T MANE Select	NP_060245.3:p.Asn376Tyr
NM_001271420.2:c.805A>T	NP_001258349.1:p.Asn269Tyr