Canonical Allele Identifier: CA2202259733

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2496318_2496319delinsGC , CM000678.2:g.2496318_2496319delinsGC	GRCh38
NC_000016.9:g.2546319_2546320delinsGC , CM000678.1:g.2546319_2546320delinsGC	GRCh37
NC_000016.8:g.2486320_2486321delinsGC	NCBI36
NG_028170.1:g.26173_26174delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000562105.2:c.170_171delinsGC	ENSP00000457896.2:p.Arg57=
ENST00000567020.6:c.170_171delinsGC	ENSP00000454408.1:p.Arg57=
ENST00000569874.2:c.170_171delinsGC	ENSP00000455005.2:p.Arg57=
ENST00000643767.1:c.170_171delinsGC	ENSP00000494145.1:p.Arg57=
ENST00000646147.1:c.170_171delinsGC MANE Select	ENSP00000494678.1:p.Arg57=
ENST00000293970.9:c.170_171delinsGC	ENSP00000293970.5:p.Arg57=
ENST00000564543.1:c.170_171delinsGC	ENSP00000455547.1:p.Arg57=
ENST00000567020.5:c.170_171delinsGC	ENSP00000454408.1:p.Arg57=
ENST00000627285.1:c.170_171delinsGC	ENSP00000486121.1:p.Arg57=
ENST00000630263.2:c.170_171delinsGC	ENSP00000486835.1:p.Arg57=
NM_001199107.1:c.170_171delinsGC	NP_001186036.1:p.Arg57=
NM_020705.2:c.170_171delinsGC	NP_065756.1:p.Arg57=
XM_017023493.1:c.170_171delinsGC	XP_016878982.1:p.Arg57=
XM_017023494.1:c.170_171delinsGC	XP_016878983.1:p.Arg57=
XM_017023495.1:c.170_171delinsGC	XP_016878984.1:p.Arg57=
XR_001751956.1:n.352_353delinsGC
NM_001199107.2:c.170_171delinsGC MANE Select	NP_001186036.1:p.Arg57=
NM_020705.3:c.170_171delinsGC	NP_065756.1:p.Arg57=