Canonical Allele Identifier: CA2202260716

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2498262T= , CM000678.2:g.2498262T=	GRCh38
NC_000016.9:g.2548263T= , CM000678.1:g.2548263T=	GRCh37
NC_000016.8:g.2488264T=	NCBI36
NG_028170.1:g.28117T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000562105.2:c.1008T=	ENSP00000457896.2:p.His336=
ENST00000567020.6:c.990T=	ENSP00000454408.1:p.His330=
ENST00000569874.2:c.990T=	ENSP00000455005.2:p.His330=
ENST00000643767.1:c.990T=	ENSP00000494145.1:p.His330=
ENST00000646147.1:c.1008T= MANE Select	ENSP00000494678.1:p.His336=
ENST00000293970.9:c.1008T=	ENSP00000293970.5:p.His336=
ENST00000564543.1:c.965+1149T=	ENSP00000455547.1:n.965+1149T=
ENST00000567020.5:c.990T=	ENSP00000454408.1:p.His330=
ENST00000627285.1:c.990T=	ENSP00000486121.1:p.His330=
ENST00000630263.2:c.986T=	ENSP00000486835.1:p.Met329=
NM_001199107.1:c.1008T=	NP_001186036.1:p.His336=
NM_020705.2:c.990T=	NP_065756.1:p.His330=
XM_017023493.1:c.1008T=	XP_016878982.1:p.His336=
XM_017023494.1:c.990T=	XP_016878983.1:p.His330=
XM_017023495.1:c.990T=	XP_016878984.1:p.His330=
XR_001751956.1:n.1190T=
NM_001199107.2:c.1008T= MANE Select	NP_001186036.1:p.His336=
NM_020705.3:c.990T=	NP_065756.1:p.His330=