Canonical Allele Identifier: CA398382065

Gene: TTC19

Linked Data

• gnomAD v4: 17-15999886-T-C
• MyVariant Identifiers: chr17:g.15903200T>C (hg19) ; chr17:g.15999886T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999886T>C , CM000679.2:g.15999886T>C	GRCh38
NC_000017.10:g.15903200T>C , CM000679.1:g.15903200T>C	GRCh37
NC_000017.9:g.15843925T>C	NCBI36
NG_029806.1:g.5507T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.38T>C MANE Select	ENSP00000261647.5:p.Phe13Ser
ENST00000261647.9:c.38T>C	ENSP00000261647.5:p.Phe13Ser
ENST00000466729.5:c.103T>C
ENST00000470399.1:c.53T>C	ENSP00000465082.1:p.Phe18Ser
ENST00000475723.5:c.85T>C
ENST00000497842.6:n.63T>C
ENST00000583704.1:n.63T>C
NM_001271420.1:c.-421T>C	NP_001258349.1:n.-421T>C
NM_017775.3:c.38T>C	NP_060245.3:p.Phe13Ser
XM_011523950.1:c.38T>C	XP_011522252.1:p.Phe13Ser
XM_017024801.2:c.38T>C	XP_016880290.2:p.Phe13Ser
XM_017024802.2:c.38T>C	XP_016880291.2:p.Phe13Ser
XM_024450814.1:c.38T>C	XP_024306582.1:p.Phe13Ser
NM_017775.4:c.38T>C MANE Select	NP_060245.3:p.Phe13Ser
NM_001271420.2:c.-421T>C	NP_001258349.1:n.-421T>C