Canonical Allele Identifier: CA398379540

Gene: TTC19

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.1126A>C MANE Select	ENSP00000261647.5:p.Asn376His
ENST00000261647.9:c.1126A>C	ENSP00000261647.5:p.Asn376His
ENST00000465567.1:n.1520A>C
ENST00000470649.1:c.247+803A>C	ENSP00000465627.1:n.247+803A>C
ENST00000475723.5:c.1310A>C
ENST00000481107.1:n.1794A>C
ENST00000497842.6:n.1330A>C
NM_001271420.1:c.805A>C	NP_001258349.1:p.Asn269His
NM_017775.3:c.1126A>C	NP_060245.3:p.Asn376His
XM_017024801.2:c.994+803A>C	XP_016880290.2:n.994+803A>C
XM_017024802.2:c.994+803A>C	XP_016880291.2:n.994+803A>C
NM_017775.4:c.1126A>C MANE Select	NP_060245.3:p.Asn376His
NM_001271420.2:c.805A>C	NP_001258349.1:p.Asn269His