Canonical Allele Identifier: CA2249815069

Gene: TTC19

Linked Data

• dbSNP Id: rs1970668922

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000067_16000089del , CM000679.2:g.16000067_16000089del	GRCh38
NC_000017.10:g.15903381_15903403del , CM000679.1:g.15903381_15903403del	GRCh37
NC_000017.9:g.15844106_15844128del	NCBI36
NG_029806.1:g.5688_5710del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.184+35_185-29del MANE Select	ENSP00000261647.5:n.184+35_185-29del
ENST00000261647.9:c.184+35_185-29del	ENSP00000261647.5:n.184+35_185-29del
ENST00000466729.5:c.249+35_250-29del
ENST00000470399.1:c.199+35_200-29del	ENSP00000465082.1:n.199+35_200-29del
ENST00000475723.5:c.231+35_232-29del
ENST00000497842.6:n.244_266del
ENST00000583704.1:n.209+35_210-29del
NM_001271420.1:c.-275+35_-274-29del	NP_001258349.1:n.-275+35_-274-29del
NM_017775.3:c.184+35_185-29del	NP_060245.3:n.184+35_185-29del
XM_011523950.1:c.184+35_185-29del	XP_011522252.1:n.184+35_185-29del
XM_017024801.2:c.184+35_185-29del	XP_016880290.2:n.184+35_185-29del
XM_017024802.2:c.184+35_185-29del	XP_016880291.2:n.184+35_185-29del
XM_024450814.1:c.184+35_185-29del	XP_024306582.1:n.184+35_185-29del
NM_017775.4:c.184+35_185-29del MANE Select	NP_060245.3:n.184+35_185-29del
NM_001271420.2:c.-275+35_-274-29del	NP_001258349.1:n.-275+35_-274-29del