Canonical Allele Identifier: CA2202259655

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2496148T= , CM000678.2:g.2496148T=	GRCh38
NC_000016.9:g.2546149T= , CM000678.1:g.2546149T=	GRCh37
NC_000016.8:g.2486150T=	NCBI36
NG_028170.1:g.26003T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000562105.2:c.-1T=	ENSP00000457896.2:n.-1T=
ENST00000567020.6:c.-1T=	ENSP00000454408.1:n.-1T=
ENST00000569874.2:c.-1T=	ENSP00000455005.2:n.-1T=
ENST00000643767.1:c.-1T=	ENSP00000494145.1:n.-1T=
ENST00000646147.1:c.-1T= MANE Select	ENSP00000494678.1:n.-1T=
ENST00000293970.9:c.-1T=	ENSP00000293970.5:n.-1T=
ENST00000562105.1:c.-1T=	ENSP00000457896.1:n.-1T=
ENST00000564543.1:c.-1T=	ENSP00000455547.1:n.-1T=
ENST00000567020.5:c.-1T=	ENSP00000454408.1:n.-1T=
ENST00000627285.1:c.-1T=	ENSP00000486121.1:n.-1T=
ENST00000630263.2:c.-1T=	ENSP00000486835.1:n.-1T=
NM_001199107.1:c.-1T=	NP_001186036.1:n.-1T=
NM_020705.2:c.-1T=	NP_065756.1:n.-1T=
XM_017023493.1:c.-1T=	XP_016878982.1:n.-1T=
XM_017023494.1:c.-1T=	XP_016878983.1:n.-1T=
XM_017023495.1:c.-1T=	XP_016878984.1:n.-1T=
XR_001751956.1:n.182T=
NM_001199107.2:c.-1T= MANE Select	NP_001186036.1:n.-1T=
NM_020705.3:c.-1T=	NP_065756.1:n.-1T=