Canonical Allele Identifier: CA385783628
Gene: TBC1D15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.71907122G>T , CM000674.2:g.71907122G>T GRCh38
NC_000012.11:g.72300902G>T , CM000674.1:g.72300902G>T GRCh37
NC_000012.10:g.70587169G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001146213.3:c.1284G>T MANE Select NP_001139685.2:p.Met428Ile
ENST00000485960.7:c.1284G>T MANE Select ENSP00000420678.2:p.Met428Ile
NM_001146213.1:c.1284G>T NP_001139685.2:p.Met428Ile
NM_001146213.2:c.1284G>T NP_001139685.2:p.Met428Ile
NM_001146214.1:c.1308G>T NP_001139686.1:p.Met436Ile
NM_001146214.2:c.1308G>T NP_001139686.1:p.Met436Ile
NM_001146214.3:c.987G>T NP_001139686.2:p.Met329Ile
NM_001385848.1:c.1284G>T NP_001372777.1:p.Met428Ile
NM_001385849.1:c.1251G>T NP_001372778.1:p.Met417Ile
NM_001385850.1:c.1284G>T NP_001372779.1:p.Met428Ile
NM_001385851.1:c.1278G>T NP_001372780.1:p.Met426Ile
NM_001385852.1:c.1209G>T NP_001372781.1:p.Met403Ile
NM_001385853.1:c.1184-6704G>T NP_001372782.1:n.1184-6704G>T
NM_001385854.1:c.1110G>T NP_001372783.1:p.Met370Ile
NM_022771.4:c.1335G>T NP_073608.4:p.Met445Ile
NM_022771.5:c.1335G>T NP_073608.4:p.Met445Ile
NM_022771.6:c.1335G>T NP_073608.4:p.Met445Ile
NR_027449.1:n.1148G>T
NR_027449.2:n.1096G>T
NR_027449.3:n.1096G>T
NR_169765.1:n.1489G>T
NR_169766.1:n.1227G>T
NR_169767.1:n.1438G>T
NR_169768.1:n.1168G>T
NR_169769.1:n.1303G>T
NR_169770.1:n.1376G>T
NR_169771.1:n.1258G>T
NR_169772.1:n.957G>T
NR_169773.1:n.1307G>T
NR_169774.1:n.1307G>T
NR_169775.1:n.1398G>T
NR_169776.1:n.1191G>T
NR_169777.1:n.1307G>T
NR_169778.1:n.1302+5G>T
NR_169779.1:n.1416G>T
NR_169780.1:n.1307G>T
NR_169781.1:n.1282G>T
NR_169782.1:n.1438G>T
NR_169783.1:n.1507G>T
NR_169784.1:n.1096G>T
NR_169785.1:n.1438G>T
NR_169786.1:n.1188G>T
NR_169787.1:n.1096G>T
NR_169788.1:n.1050G>T
NR_169789.1:n.1136G>T
ENST00000319106.12:c.1308G>T ENSP00000318262.6:p.Met436Ile
ENST00000462788.6:c.*698G>T ENSP00000418467.2:n.*698G>T
ENST00000479971.1:n.196G>T
ENST00000483828.6:n.589G>T
ENST00000485960.6:c.1284G>T ENSP00000420678.2:p.Met428Ile
ENST00000548679.5:n.266G>T
ENST00000550746.5:c.1335G>T ENSP00000448182.1:p.Met445Ile
XM_006719564.2:c.1359G>T XP_006719627.1:p.Met453Ile
XM_006719565.2:c.1308G>T XP_006719628.1:p.Met436Ile
XM_006719565.4:c.1308G>T XP_006719628.1:p.Met436Ile
XM_006719566.2:c.1038G>T XP_006719629.1:p.Met346Ile
XM_006719566.3:c.1038G>T XP_006719629.1:p.Met346Ile
XM_006719567.2:c.597G>T XP_006719630.1:p.Met199Ile
XM_011538679.1:c.1038G>T XP_011536981.1:p.Met346Ile
XM_011538680.1:c.1038G>T XP_011536982.1:p.Met346Ile
XM_011538681.1:c.1335G>T XP_011536983.1:p.Met445Ile
XM_011538681.3:c.1335G>T XP_011536983.1:p.Met445Ile
XM_011538682.1:c.597G>T XP_011536984.1:p.Met199Ile
XM_011538683.1:c.597G>T XP_011536985.1:p.Met199Ile
XM_017019825.1:c.987G>T XP_016875314.1:p.Met329Ile
XM_017019827.1:c.903G>T XP_016875316.1:p.Met301Ile
XM_017019828.1:c.852G>T XP_016875317.1:p.Met284Ile