Canonical Allele Identifier: CA624961167

Gene: TTC19

Linked Data

• dbSNP Id: rs1413254899
• gnomAD v2: 17-15903144-C-T
• gnomAD v3: 17-15999830-C-T
• gnomAD v4: 17-15999830-C-T
• MyVariant Identifiers: chr17:g.15903144C>T (hg19) ; chr17:g.15999830C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999830C>T , CM000679.2:g.15999830C>T	GRCh38
NC_000017.10:g.15903144C>T , CM000679.1:g.15903144C>T	GRCh37
NC_000017.9:g.15843869C>T	NCBI36
NG_029806.1:g.5451C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.-19C>T MANE Select	ENSP00000261647.5:n.-19C>T
ENST00000261647.9:c.-19C>T	ENSP00000261647.5:n.-19C>T
ENST00000466729.5:c.47C>T
ENST00000475723.5:c.29C>T
ENST00000497842.6:n.7C>T
ENST00000583704.1:n.7C>T
NM_001271420.1:c.-477C>T	NP_001258349.1:n.-477C>T
NM_017775.3:c.-19C>T	NP_060245.3:n.-19C>T
XM_011523950.1:c.-19C>T	XP_011522252.1:n.-19C>T
XM_017024801.2:c.-19C>T	XP_016880290.2:n.-19C>T
XM_017024802.2:c.-19C>T	XP_016880291.2:n.-19C>T
XM_024450814.1:c.-19C>T	XP_024306582.1:n.-19C>T
NM_017775.4:c.-19C>T MANE Select	NP_060245.3:n.-19C>T
NM_001271420.2:c.-477C>T	NP_001258349.1:n.-477C>T