Canonical Allele Identifier: CA2202262024

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2500822C= , CM000678.2:g.2500822C=	GRCh38
NC_000016.9:g.2550823C= , CM000678.1:g.2550823C=	GRCh37
NC_000016.8:g.2490824C=	NCBI36
NG_028170.1:g.30677C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567020.6:c.1526C=	ENSP00000454408.1:p.Ala509=
ENST00000569874.2:c.1526C=	ENSP00000455005.2:p.Ala509=
ENST00000646147.1:c.1544C= MANE Select	ENSP00000494678.1:p.Ala515=
ENST00000293970.9:c.1544C=	ENSP00000293970.5:p.Ala515=
ENST00000564543.1:c.965+3709C=	ENSP00000455547.1:n.965+3709C=
ENST00000564879.2:c.413C=
ENST00000567020.5:c.1526C=	ENSP00000454408.1:p.Ala509=
ENST00000627285.1:c.1526C=	ENSP00000486121.1:p.Ala509=
ENST00000630263.2:c.*502C=	ENSP00000486835.1:n.*502C=
NM_001199107.1:c.1544C=	NP_001186036.1:p.Ala515=
NM_020705.2:c.1526C=	NP_065756.1:p.Ala509=
XM_017023493.1:c.1544C=	XP_016878982.1:p.Ala515=
XM_017023494.1:c.1526C=	XP_016878983.1:p.Ala509=
XM_017023495.1:c.1526C=	XP_016878984.1:p.Ala509=
XR_001751956.1:n.1726C=
NM_001199107.2:c.1544C= MANE Select	NP_001186036.1:p.Ala515=
NM_020705.3:c.1526C=	NP_065756.1:p.Ala509=