Canonical Allele Identifier: CA2739521143

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.15999778A>C , CM000679.2:g.15999778A>C	GRCh38
NC_000017.10:g.15903092A>C , CM000679.1:g.15903092A>C	GRCh37
NC_000017.9:g.15843817A>C	NCBI36
NG_029806.1:g.5399A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.9:c.-71A>C	ENSP00000261647.5:n.-71A>C
NM_001271420.1:c.-529A>C	NP_001258349.1:n.-529A>C
NM_017775.3:c.-71A>C	NP_060245.3:n.-71A>C
XM_011523950.1:c.-71A>C	XP_011522252.1:n.-71A>C
XM_017024801.2:c.-71A>C	XP_016880290.2:n.-71A>C
XM_017024802.2:c.-71A>C	XP_016880291.2:n.-71A>C
XM_024450814.1:c.-71A>C	XP_024306582.1:n.-71A>C