Canonical Allele Identifier: CA2202249371

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2501235C= , CM000678.2:g.2501235C=	GRCh38
NC_000016.9:g.2551236C= , CM000678.1:g.2551236C=	GRCh37
NC_000016.8:g.2491237C=	NCBI36
NG_028170.1:g.31090C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001199107.2:c.*277C= MANE Select	NP_001186036.1:n.*277C=
ENST00000646147.1:c.*277C= MANE Select	ENSP00000494678.1:n.*277C=
NM_001199107.1:c.*277C=	NP_001186036.1:n.*277C=
NM_020705.2:c.*277C=	NP_065756.1:n.*277C=
NM_020705.3:c.*277C=	NP_065756.1:n.*277C=
ENST00000293970.9:c.*277C=	ENSP00000293970.5:n.*277C=
ENST00000564543.1:c.965+4122C=	ENSP00000455547.1:n.965+4122C=
ENST00000564879.2:c.826C=
ENST00000567020.5:c.*277C=	ENSP00000454408.1:n.*277C=
ENST00000567020.6:c.*277C=	ENSP00000454408.1:n.*277C=
ENST00000569874.1:c.154+183C=	ENSP00000455005.1:n.154+183C=
ENST00000569874.2:c.*94+183C=	ENSP00000455005.2:n.*94+183C=
ENST00000627285.1:c.*277C=	ENSP00000486121.1:n.*277C=
ENST00000630263.2:c.*915C=	ENSP00000486835.1:n.*915C=
XM_017023493.1:c.*14+263C=	XP_016878982.1:n.*14+263C=
XM_017023494.1:c.*277C=	XP_016878983.1:n.*277C=
XM_017023495.1:c.*14+263C=	XP_016878984.1:n.*14+263C=
XR_001751956.1:n.2139C=