Canonical Allele Identifier: CA394377246
Gene: TBC1D24 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2496918G>T , CM000678.2:g.2496918G>T GRCh38
NC_000016.9:g.2546919G>T , CM000678.1:g.2546919G>T GRCh37
NC_000016.8:g.2486920G>T NCBI36
NG_028170.1:g.26773G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000562105.2:c.770G>T ENSP00000457896.2:p.Gly257Val
ENST00000567020.6:c.770G>T ENSP00000454408.1:p.Gly257Val
ENST00000569874.2:c.770G>T ENSP00000455005.2:p.Gly257Val
ENST00000643767.1:c.770G>T ENSP00000494145.1:p.Gly257Val
ENST00000646147.1:c.770G>T MANE Select ENSP00000494678.1:p.Gly257Val
ENST00000293970.9:c.770G>T ENSP00000293970.5:p.Gly257Val
ENST00000564543.1:c.770G>T ENSP00000455547.1:p.Gly257Val
ENST00000567020.5:c.770G>T ENSP00000454408.1:p.Gly257Val
ENST00000627285.1:c.770G>T ENSP00000486121.1:p.Gly257Val
ENST00000630263.2:c.770G>T ENSP00000486835.1:p.Gly257Val
NM_001199107.1:c.770G>T NP_001186036.1:p.Gly257Val
NM_020705.2:c.770G>T NP_065756.1:p.Gly257Val
XM_017023493.1:c.770G>T XP_016878982.1:p.Gly257Val
XM_017023494.1:c.770G>T XP_016878983.1:p.Gly257Val
XM_017023495.1:c.770G>T XP_016878984.1:p.Gly257Val
XR_001751956.1:n.952G>T
NM_001199107.2:c.770G>T MANE Select NP_001186036.1:p.Gly257Val
NM_020705.3:c.770G>T NP_065756.1:p.Gly257Val