Canonical Allele Identifier: CA394376854
Gene: TBC1D24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2496809C>G , CM000678.2:g.2496809C>G GRCh38
NC_000016.9:g.2546810C>G , CM000678.1:g.2546810C>G GRCh37
NC_000016.8:g.2486811C>G NCBI36
NG_028170.1:g.26664C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000562105.2:c.661C>G ENSP00000457896.2:p.Pro221Ala
ENST00000567020.6:c.661C>G ENSP00000454408.1:p.Pro221Ala
ENST00000569874.2:c.661C>G ENSP00000455005.2:p.Pro221Ala
ENST00000643767.1:c.661C>G ENSP00000494145.1:p.Pro221Ala
ENST00000646147.1:c.661C>G MANE Select ENSP00000494678.1:p.Pro221Ala
ENST00000293970.9:c.661C>G ENSP00000293970.5:p.Pro221Ala
ENST00000564543.1:c.661C>G ENSP00000455547.1:p.Pro221Ala
ENST00000567020.5:c.661C>G ENSP00000454408.1:p.Pro221Ala
ENST00000627285.1:c.661C>G ENSP00000486121.1:p.Pro221Ala
ENST00000630263.2:c.661C>G ENSP00000486835.1:p.Pro221Ala
NM_001199107.1:c.661C>G NP_001186036.1:p.Pro221Ala
NM_020705.2:c.661C>G NP_065756.1:p.Pro221Ala
XM_017023493.1:c.661C>G XP_016878982.1:p.Pro221Ala
XM_017023494.1:c.661C>G XP_016878983.1:p.Pro221Ala
XM_017023495.1:c.661C>G XP_016878984.1:p.Pro221Ala
XR_001751956.1:n.843C>G
NM_001199107.2:c.661C>G MANE Select NP_001186036.1:p.Pro221Ala
NM_020705.3:c.661C>G NP_065756.1:p.Pro221Ala