Canonical Allele Identifier: CA2249871118

Gene: TTC19

Linked Data

• dbSNP Id: rs1971661824
• gnomAD v4: 17-16028455-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16028455T>C , CM000679.2:g.16028455T>C	GRCh38
NC_000017.10:g.15931769T>C , CM000679.1:g.15931769T>C	GRCh37
NC_000017.9:g.15872494T>C	NCBI36
NG_029806.1:g.34076T>C
NG_047111.1:g.193292A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*933T>C MANE Select	ENSP00000261647.5:n.*933T>C
ENST00000261647.9:c.*933T>C	ENSP00000261647.5:n.*933T>C
ENST00000465567.1:n.2470T>C
ENST00000470649.1:c.247+1753T>C	ENSP00000465627.1:n.247+1753T>C
ENST00000475723.5:c.2260T>C
ENST00000481107.1:n.2744T>C
NM_001271420.1:c.*933T>C	NP_001258349.1:n.*933T>C
NM_017775.3:c.*933T>C	NP_060245.3:n.*933T>C
XM_017024801.2:c.994+1753T>C	XP_016880290.2:n.994+1753T>C
XM_017024802.2:c.994+1753T>C	XP_016880291.2:n.994+1753T>C
NM_017775.4:c.*933T>C MANE Select	NP_060245.3:n.*933T>C
NM_001271420.2:c.*933T>C	NP_001258349.1:n.*933T>C