Canonical Allele Identifier: CA8407628

Gene: TTC19

Linked Data

• dbSNP Id: rs753495260
• ExAC: 17:15930927 C / A
• gnomAD v2: 17-15930927-C-A
• gnomAD v4: 17-16027613-C-A
• MyVariant Identifiers: chr17:g.15930927C>A (hg19) ; chr17:g.16027613C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16027613C>A , CM000679.2:g.16027613C>A	GRCh38
NC_000017.10:g.15930927C>A , CM000679.1:g.15930927C>A	GRCh37
NC_000017.9:g.15871652C>A	NCBI36
NG_029806.1:g.33234C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.*91C>A MANE Select	ENSP00000261647.5:n.*91C>A
ENST00000261647.9:c.*91C>A	ENSP00000261647.5:n.*91C>A
ENST00000465567.1:n.1628C>A
ENST00000470649.1:c.247+911C>A	ENSP00000465627.1:n.247+911C>A
ENST00000475723.5:c.1418C>A
ENST00000481107.1:n.1902C>A
NM_001271420.1:c.*91C>A	NP_001258349.1:n.*91C>A
NM_017775.3:c.*91C>A	NP_060245.3:n.*91C>A
XM_017024801.2:c.994+911C>A	XP_016880290.2:n.994+911C>A
XM_017024802.2:c.994+911C>A	XP_016880291.2:n.994+911C>A
NM_017775.4:c.*91C>A MANE Select	NP_060245.3:n.*91C>A
NM_001271420.2:c.*91C>A	NP_001258349.1:n.*91C>A