Canonical Allele Identifier: CA2249870105

Gene: TTC19

Linked Data

• dbSNP Id: rs1971621119

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027675T>C , CM000679.2:g.16027675T>C	GRCh38
NC_000017.10:g.15930989T>C , CM000679.1:g.15930989T>C	GRCh37
NC_000017.9:g.15871714T>C	NCBI36
NG_029806.1:g.33296T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*153T>C MANE Select	ENSP00000261647.5:n.*153T>C
ENST00000261647.9:c.*153T>C	ENSP00000261647.5:n.*153T>C
ENST00000465567.1:n.1690T>C
ENST00000470649.1:c.247+973T>C	ENSP00000465627.1:n.247+973T>C
ENST00000475723.5:c.1480T>C
ENST00000481107.1:n.1964T>C
NM_001271420.1:c.*153T>C	NP_001258349.1:n.*153T>C
NM_017775.3:c.*153T>C	NP_060245.3:n.*153T>C
XM_017024801.2:c.994+973T>C	XP_016880290.2:n.994+973T>C
XM_017024802.2:c.994+973T>C	XP_016880291.2:n.994+973T>C
NM_017775.4:c.*153T>C MANE Select	NP_060245.3:n.*153T>C
NM_001271420.2:c.*153T>C	NP_001258349.1:n.*153T>C