Canonical Allele Identifier: CA3173901837
Gene: MASTL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.27161130G= , CM000672.2:g.27161130G= GRCh38
NC_000010.10:g.27450059G= , CM000672.1:g.27450059G= GRCh37
NC_000010.9:g.27490065G= NCBI36
NG_016987.1:g.11307G=

Transcript Alleles

HGVS Amino-acid Change
NM_001172303.3:c.501G= MANE Select NP_001165774.1:p.Glu167=
ENST00000375940.9:c.501G= MANE Select ENSP00000365107.5:p.Glu167=
NM_001172303.1:c.501G= NP_001165774.1:p.Glu167=
NM_001172303.2:c.501G= NP_001165774.1:p.Glu167=
NM_001172304.1:c.501G= NP_001165775.1:p.Glu167=
NM_001172304.2:c.501G= NP_001165775.1:p.Glu167=
NM_001172304.3:c.501G= NP_001165775.1:p.Glu167=
NM_001320756.1:c.501G= NP_001307685.1:p.Glu167=
NM_001320756.2:c.501G= NP_001307685.1:p.Glu167=
NM_001320757.1:c.501G= NP_001307686.1:p.Glu167=
NM_001320757.2:c.501G= NP_001307686.1:p.Glu167=
NM_001372029.1:c.18G= NP_001358958.1:p.Glu6=
NM_001372030.1:c.18G= NP_001358959.1:p.Glu6=
NM_032844.3:c.501G= NP_116233.2:p.Glu167=
NM_032844.4:c.501G= NP_116233.2:p.Glu167=
NM_032844.5:c.501G= NP_116233.2:p.Glu167=
NR_135469.1:n.1104G=
NR_135469.2:n.576G=
ENST00000342386.10:c.501G= ENSP00000343446.5:p.Glu167=
ENST00000375940.8:c.501G= ENSP00000365107.4:p.Glu167=
ENST00000375946.8:c.501G= ENSP00000365113.4:p.Glu167=
XM_005252630.2:c.501G= XP_005252687.1:p.Glu167=
XM_005252631.2:c.501G= XP_005252688.1:p.Glu167=
XM_005252631.4:c.501G= XP_005252688.1:p.Glu167=
XM_005252632.2:c.501G= XP_005252689.1:p.Glu167=
XM_005252632.4:c.501G= XP_005252689.1:p.Glu167=
XM_006717518.2:c.501G= XP_006717581.1:p.Glu167=
XM_006717519.2:c.501G= XP_006717582.1:p.Glu167=
XM_006717519.4:c.501G= XP_006717582.1:p.Glu167=
XM_006717520.2:c.501G= XP_006717583.1:p.Glu167=
XM_006717520.4:c.501G= XP_006717583.1:p.Glu167=
XM_017016852.2:c.501G= XP_016872341.1:p.Glu167=
XM_017016853.2:c.354G= XP_016872342.1:p.Glu118=
XM_017016855.2:c.501G= XP_016872344.1:p.Glu167=
XM_017016856.2:c.501G= XP_016872345.1:p.Glu167=
XM_024448243.1:c.501G= XP_024304011.1:p.Glu167=
XM_024448244.1:c.501G= XP_024304012.1:p.Glu167=
XR_930523.1:n.576G=