Canonical Allele Identifier: CA5746103
Gene: MKI67 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.128103952T>C , CM000672.2:g.128103952T>C GRCh38
NC_000010.10:g.129902216T>C , CM000672.1:g.129902216T>C GRCh37
NC_000010.9:g.129792206T>C NCBI36
NG_047061.1:g.27412A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368654.8:c.7888A>G MANE Select ENSP00000357643.3:p.Thr2630Ala
ENST00000368653.7:c.6808A>G ENSP00000357642.3:p.Thr2270Ala
ENST00000368654.7:c.7888A>G ENSP00000357643.3:p.Thr2630Ala
ENST00000617118.1:c.7885A>G ENSP00000479215.1:p.Thr2629Ala
NM_001145966.1:c.6808A>G NP_001139438.1:p.Thr2270Ala
NM_002417.4:c.7888A>G NP_002408.3:p.Thr2630Ala
XM_006717864.2:c.5566A>G XP_006717927.2:p.Thr1856Ala
XM_011539818.1:c.6856A>G XP_011538120.1:p.Thr2286Ala
XM_006717864.3:c.5566A>G XP_006717927.2:p.Thr1856Ala
XM_011539818.2:c.6856A>G XP_011538120.1:p.Thr2286Ala
NM_002417.5:c.7888A>G MANE Select NP_002408.3:p.Thr2630Ala
NM_001145966.2:c.6808A>G NP_001139438.1:p.Thr2270Ala