Canonical Allele Identifier: CA919799544
Gene: TTC19 HGNC NCBI

Linked Data

dbSNP Id: rs1597446322

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.15999820_15999852del , CM000679.2:g.15999820_15999852del GRCh38
NC_000017.10:g.15903134_15903166del , CM000679.1:g.15903134_15903166del GRCh37
NC_000017.9:g.15843859_15843891del NCBI36
NG_029806.1:g.5441_5473del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.9:c.-29_4del
ENST00000466729.5:c.37_69del
ENST00000475723.5:c.19_51del
NM_001271420.1:c.-487_-455del NP_001258349.1:n.-487_-455del
NM_017775.3:c.-29_4del
XM_011523950.1:c.-29_4del
XM_017024801.2:c.-29_4del
XM_017024802.2:c.-29_4del
XM_024450814.1:c.-29_4del