Canonical Allele Identifier: CA2739521159

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999816T>G , CM000679.2:g.15999816T>G	GRCh38
NC_000017.10:g.15903130T>G , CM000679.1:g.15903130T>G	GRCh37
NC_000017.9:g.15843855T>G	NCBI36
NG_029806.1:g.5437T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-33T>G	ENSP00000261647.5:n.-33T>G
ENST00000466729.5:c.33T>G
ENST00000475723.5:c.15T>G
NM_001271420.1:c.-491T>G	NP_001258349.1:n.-491T>G
NM_017775.3:c.-33T>G	NP_060245.3:n.-33T>G
XM_011523950.1:c.-33T>G	XP_011522252.1:n.-33T>G
XM_017024801.2:c.-33T>G	XP_016880290.2:n.-33T>G
XM_017024802.2:c.-33T>G	XP_016880291.2:n.-33T>G
XM_024450814.1:c.-33T>G	XP_024306582.1:n.-33T>G