Canonical Allele Identifier: CA394381435

Gene: TBC1D24

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2500802A>C , CM000678.2:g.2500802A>C	GRCh38
NC_000016.9:g.2550803A>C , CM000678.1:g.2550803A>C	GRCh37
NC_000016.8:g.2490804A>C	NCBI36
NG_028170.1:g.30657A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001199107.2:c.1526-2A>C MANE Select	NP_001186036.1:n.1526-2A>C
ENST00000646147.1:c.1526-2A>C MANE Select	ENSP00000494678.1:n.1526-2A>C
NM_001199107.1:c.1526-2A>C	NP_001186036.1:n.1526-2A>C
NM_020705.2:c.1508-2A>C	NP_065756.1:n.1508-2A>C
NM_020705.3:c.1508-2A>C	NP_065756.1:n.1508-2A>C
ENST00000293970.9:c.1526-2A>C	ENSP00000293970.5:n.1526-2A>C
ENST00000564543.1:c.965+3689A>C	ENSP00000455547.1:n.965+3689A>C
ENST00000564879.2:c.395-2A>C
ENST00000567020.5:c.1508-2A>C	ENSP00000454408.1:n.1508-2A>C
ENST00000567020.6:c.1508-2A>C	ENSP00000454408.1:n.1508-2A>C
ENST00000569874.2:c.1508-2A>C	ENSP00000455005.2:n.1508-2A>C
ENST00000627285.1:c.1508-2A>C	ENSP00000486121.1:n.1508-2A>C
ENST00000630263.2:c.*484-2A>C	ENSP00000486835.1:n.*484-2A>C
XM_017023493.1:c.1526-2A>C	XP_016878982.1:n.1526-2A>C
XM_017023494.1:c.1508-2A>C	XP_016878983.1:n.1508-2A>C
XM_017023495.1:c.1508-2A>C	XP_016878984.1:n.1508-2A>C
XR_001751956.1:n.1708-2A>C