Canonical Allele Identifier: CA726463936

Gene: TTC19

Linked Data

• dbSNP Id: rs1190877718
• MyVariant Identifiers: chr17:g.15931546G>C (hg19) ; chr17:g.16028232G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028232G>C , CM000679.2:g.16028232G>C	GRCh38
NC_000017.10:g.15931546G>C , CM000679.1:g.15931546G>C	GRCh37
NC_000017.9:g.15872271G>C	NCBI36
NG_029806.1:g.33853G>C
NG_047111.1:g.193515C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000261647.10:c.*710G>C MANE Select	ENSP00000261647.5:n.*710G>C
ENST00000261647.9:c.*710G>C	ENSP00000261647.5:n.*710G>C
ENST00000465567.1:n.2247G>C
ENST00000470649.1:c.247+1530G>C	ENSP00000465627.1:n.247+1530G>C
ENST00000475723.5:c.2037G>C
ENST00000481107.1:n.2521G>C
NM_001271420.1:c.*710G>C	NP_001258349.1:n.*710G>C
NM_017775.3:c.*710G>C	NP_060245.3:n.*710G>C
XM_017024801.2:c.994+1530G>C	XP_016880290.2:n.994+1530G>C
XM_017024802.2:c.994+1530G>C	XP_016880291.2:n.994+1530G>C
NM_017775.4:c.*710G>C MANE Select	NP_060245.3:n.*710G>C
NM_001271420.2:c.*710G>C	NP_001258349.1:n.*710G>C