Canonical Allele Identifier: CA2249815067

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000058C= , CM000679.2:g.16000058C=	GRCh38
NC_000017.10:g.15903372C= , CM000679.1:g.15903372C=	GRCh37
NC_000017.9:g.15844097C=	NCBI36
NG_029806.1:g.5679C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.184+26C= MANE Select	ENSP00000261647.5:n.184+26C=
ENST00000261647.9:c.184+26C=	ENSP00000261647.5:n.184+26C=
ENST00000466729.5:c.249+26C=
ENST00000470399.1:c.199+26C=	ENSP00000465082.1:n.199+26C=
ENST00000475723.5:c.231+26C=
ENST00000497842.6:n.235C=
ENST00000583704.1:n.209+26C=
NM_001271420.1:c.-275+26C=	NP_001258349.1:n.-275+26C=
NM_017775.3:c.184+26C=	NP_060245.3:n.184+26C=
XM_011523950.1:c.184+26C=	XP_011522252.1:n.184+26C=
XM_017024801.2:c.184+26C=	XP_016880290.2:n.184+26C=
XM_017024802.2:c.184+26C=	XP_016880291.2:n.184+26C=
XM_024450814.1:c.184+26C=	XP_024306582.1:n.184+26C=
NM_017775.4:c.184+26C= MANE Select	NP_060245.3:n.184+26C=
NM_001271420.2:c.-275+26C=	NP_001258349.1:n.-275+26C=