Canonical Allele Identifier: CA7844291

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2500390C>T , CM000678.2:g.2500390C>T	GRCh38
NC_000016.9:g.2550391C>T , CM000678.1:g.2550391C>T	GRCh37
NC_000016.8:g.2490392C>T	NCBI36
NG_028170.1:g.30245C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000567020.6:c.1407C>T	ENSP00000454408.1:p.Pro469=
ENST00000569874.2:c.1407C>T	ENSP00000455005.2:p.Pro469=
ENST00000646147.1:c.1425C>T MANE Select	ENSP00000494678.1:p.Pro475=
ENST00000293970.9:c.1425C>T	ENSP00000293970.5:p.Pro475=
ENST00000564543.1:c.965+3277C>T	ENSP00000455547.1:n.965+3277C>T
ENST00000564879.2:c.294C>T
ENST00000567020.5:c.1407C>T	ENSP00000454408.1:p.Pro469=
ENST00000627285.1:c.1407C>T	ENSP00000486121.1:p.Pro469=
ENST00000630263.2:c.*383C>T	ENSP00000486835.1:n.*383C>T
NM_001199107.1:c.1425C>T	NP_001186036.1:p.Pro475=
NM_020705.2:c.1407C>T	NP_065756.1:p.Pro469=
XM_017023493.1:c.1425C>T	XP_016878982.1:p.Pro475=
XM_017023494.1:c.1407C>T	XP_016878983.1:p.Pro469=
XM_017023495.1:c.1407C>T	XP_016878984.1:p.Pro469=
XR_001751956.1:n.1607C>T
NM_001199107.2:c.1425C>T MANE Select	NP_001186036.1:p.Pro475=
NM_020705.3:c.1407C>T	NP_065756.1:p.Pro469=