Canonical Allele Identifier: CA2249815041

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000030C= , CM000679.2:g.16000030C=	GRCh38
NC_000017.10:g.15903344C= , CM000679.1:g.15903344C=	GRCh37
NC_000017.9:g.15844069C=	NCBI36
NG_029806.1:g.5651C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.182C= MANE Select	ENSP00000261647.5:p.Ala61=
ENST00000261647.9:c.182C=	ENSP00000261647.5:p.Ala61=
ENST00000466729.5:c.247C=
ENST00000470399.1:c.197C=	ENSP00000465082.1:p.Ala66=
ENST00000475723.5:c.229C=
ENST00000497842.6:n.207C=
ENST00000583704.1:n.207C=
NM_001271420.1:c.-277C=	NP_001258349.1:n.-277C=
NM_017775.3:c.182C=	NP_060245.3:p.Ala61=
XM_011523950.1:c.182C=	XP_011522252.1:p.Ala61=
XM_017024801.2:c.182C=	XP_016880290.2:p.Ala61=
XM_017024802.2:c.182C=	XP_016880291.2:p.Ala61=
XM_024450814.1:c.182C=	XP_024306582.1:p.Ala61=
NM_017775.4:c.182C= MANE Select	NP_060245.3:p.Ala61=
NM_001271420.2:c.-277C=	NP_001258349.1:n.-277C=