Canonical Allele Identifier: CA398382070

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999887-C-A
• MyVariant Identifiers: chr17:g.15903201C>A (hg19) ; chr17:g.15999887C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999887C>A , CM000679.2:g.15999887C>A	GRCh38
NC_000017.10:g.15903201C>A , CM000679.1:g.15903201C>A	GRCh37
NC_000017.9:g.15843926C>A	NCBI36
NG_029806.1:g.5508C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.39C>A MANE Select	ENSP00000261647.5:p.Phe13Leu
ENST00000261647.9:c.39C>A	ENSP00000261647.5:p.Phe13Leu
ENST00000466729.5:c.104C>A
ENST00000470399.1:c.54C>A	ENSP00000465082.1:p.Phe18Leu
ENST00000475723.5:c.86C>A
ENST00000497842.6:n.64C>A
ENST00000583704.1:n.64C>A
NM_001271420.1:c.-420C>A	NP_001258349.1:n.-420C>A
NM_017775.3:c.39C>A	NP_060245.3:p.Phe13Leu
XM_011523950.1:c.39C>A	XP_011522252.1:p.Phe13Leu
XM_017024801.2:c.39C>A	XP_016880290.2:p.Phe13Leu
XM_017024802.2:c.39C>A	XP_016880291.2:p.Phe13Leu
XM_024450814.1:c.39C>A	XP_024306582.1:p.Phe13Leu
NM_017775.4:c.39C>A MANE Select	NP_060245.3:p.Phe13Leu
NM_001271420.2:c.-420C>A	NP_001258349.1:n.-420C>A