Canonical Allele Identifier: CA2636259708

Gene: TTC19

Linked Data

• gnomAD v4: 17-16000042-GCGGGCCGGGCGGGGCCGGCCGGGCGGGGACAGGGGCGCGGGC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000049_16000090del , CM000679.2:g.16000049_16000090del	GRCh38
NC_000017.10:g.15903363_15903404del , CM000679.1:g.15903363_15903404del	GRCh37
NC_000017.9:g.15844088_15844129del	NCBI36
NG_029806.1:g.5670_5711del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.184+17_185-28del MANE Select	ENSP00000261647.5:n.184+17_185-28del
ENST00000261647.9:c.184+17_185-28del	ENSP00000261647.5:n.184+17_185-28del
ENST00000466729.5:c.249+17_250-28del
ENST00000470399.1:c.199+17_200-28del	ENSP00000465082.1:n.199+17_200-28del
ENST00000475723.5:c.231+17_232-28del
ENST00000497842.6:n.226_267del
ENST00000583704.1:n.209+17_210-28del
NM_001271420.1:c.-275+17_-274-28del	NP_001258349.1:n.-275+17_-274-28del
NM_017775.3:c.184+17_185-28del	NP_060245.3:n.184+17_185-28del
XM_011523950.1:c.184+17_185-28del	XP_011522252.1:n.184+17_185-28del
XM_017024801.2:c.184+17_185-28del	XP_016880290.2:n.184+17_185-28del
XM_017024802.2:c.184+17_185-28del	XP_016880291.2:n.184+17_185-28del
XM_024450814.1:c.184+17_185-28del	XP_024306582.1:n.184+17_185-28del
NM_017775.4:c.184+17_185-28del MANE Select	NP_060245.3:n.184+17_185-28del
NM_001271420.2:c.-275+17_-274-28del	NP_001258349.1:n.-275+17_-274-28del