Canonical Allele Identifier: CA2249815042

Gene: TTC19

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.16000032G= , CM000679.2:g.16000032G=	GRCh38
NC_000017.10:g.15903346G= , CM000679.1:g.15903346G=	GRCh37
NC_000017.9:g.15844071G=	NCBI36
NG_029806.1:g.5653G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261647.10:c.184G= MANE Select	ENSP00000261647.5:p.Ala62=
ENST00000261647.9:c.184G=	ENSP00000261647.5:p.Ala62=
ENST00000466729.5:c.249G=
ENST00000470399.1:c.199G=	ENSP00000465082.1:p.Ala67=
ENST00000475723.5:c.231G=
ENST00000497842.6:n.209G=
ENST00000583704.1:n.209G=
NM_001271420.1:c.-275G=	NP_001258349.1:n.-275G=
NM_017775.3:c.184G=	NP_060245.3:p.Ala62=
XM_011523950.1:c.184G=	XP_011522252.1:p.Ala62=
XM_017024801.2:c.184G=	XP_016880290.2:p.Ala62=
XM_017024802.2:c.184G=	XP_016880291.2:p.Ala62=
XM_024450814.1:c.184G=	XP_024306582.1:p.Ala62=
NM_017775.4:c.184G= MANE Select	NP_060245.3:p.Ala62=
NM_001271420.2:c.-275G=	NP_001258349.1:n.-275G=