Canonical Allele Identifier: CA10647233

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2500944C>G , CM000678.2:g.2500944C>G	GRCh38
NC_000016.9:g.2550945C>G , CM000678.1:g.2550945C>G	GRCh37
NC_000016.8:g.2490946C>G	NCBI36
NG_028170.1:g.30799C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567020.6:c.1648C>G	ENSP00000454408.1:p.Pro550Ala
ENST00000569874.2:c.1648C>G	ENSP00000455005.2:p.Pro550Ala
ENST00000646147.1:c.1666C>G MANE Select	ENSP00000494678.1:p.Pro556Ala
ENST00000293970.9:c.1666C>G	ENSP00000293970.5:p.Pro556Ala
ENST00000564543.1:c.965+3831C>G	ENSP00000455547.1:n.965+3831C>G
ENST00000564879.2:c.535C>G
ENST00000567020.5:c.1648C>G	ENSP00000454408.1:p.Pro550Ala
ENST00000569874.1:c.46C>G	ENSP00000455005.1:p.Pro16Ala
ENST00000627285.1:c.1648C>G	ENSP00000486121.1:p.Pro550Ala
ENST00000630263.2:c.*624C>G	ENSP00000486835.1:n.*624C>G
NM_001199107.1:c.1666C>G	NP_001186036.1:p.Pro556Ala
NM_020705.2:c.1648C>G	NP_065756.1:p.Pro550Ala
XM_017023493.1:c.1666C>G	XP_016878982.1:p.Pro556Ala
XM_017023494.1:c.1648C>G	XP_016878983.1:p.Pro550Ala
XM_017023495.1:c.1648C>G	XP_016878984.1:p.Pro550Ala
XR_001751956.1:n.1848C>G
NM_001199107.2:c.1666C>G MANE Select	NP_001186036.1:p.Pro556Ala
NM_020705.3:c.1648C>G	NP_065756.1:p.Pro550Ala