Canonical Allele Identifier: CA981845647
Gene: TTC19 HGNC NCBI

Linked Data

dbSNP Id: rs1970668605

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.16000056_16000065dup , CM000679.2:g.16000056_16000065dup GRCh38
NC_000017.10:g.15903370_15903379dup , CM000679.1:g.15903370_15903379dup GRCh37
NC_000017.9:g.15844095_15844104dup NCBI36
NG_029806.1:g.5677_5686dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000261647.10:c.184+24_184+33dup MANE Select ENSP00000261647.5:n.184+24_184+33dup
ENST00000261647.9:c.184+24_184+33dup ENSP00000261647.5:n.184+24_184+33dup
ENST00000466729.5:c.249+24_249+33dup
ENST00000470399.1:c.199+24_199+33dup ENSP00000465082.1:n.199+24_199+33dup
ENST00000475723.5:c.231+24_231+33dup
ENST00000497842.6:n.233_242dup
ENST00000583704.1:n.209+24_209+33dup
NM_001271420.1:c.-275+24_-275+33dup NP_001258349.1:n.-275+24_-275+33dup
NM_017775.3:c.184+24_184+33dup NP_060245.3:n.184+24_184+33dup
XM_011523950.1:c.184+24_184+33dup XP_011522252.1:n.184+24_184+33dup
XM_017024801.2:c.184+24_184+33dup XP_016880290.2:n.184+24_184+33dup
XM_017024802.2:c.184+24_184+33dup XP_016880291.2:n.184+24_184+33dup
XM_024450814.1:c.184+24_184+33dup XP_024306582.1:n.184+24_184+33dup
NM_017775.4:c.184+24_184+33dup MANE Select NP_060245.3:n.184+24_184+33dup
NM_001271420.2:c.-275+24_-275+33dup NP_001258349.1:n.-275+24_-275+33dup