Canonical Allele Identifier: CA404791541
Gene: MAST3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.18144519C>T , CM000681.2:g.18144519C>T GRCh38
NC_000019.9:g.18255329C>T , CM000681.1:g.18255329C>T GRCh37
NC_000019.8:g.18116329C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000697700.2:c.2572C>T ENSP00000513407.2:p.Arg858Ter
ENST00000697701.1:c.2617C>T ENSP00000513408.1:p.Arg873Ter
ENST00000697702.1:c.2569C>T ENSP00000513409.1:p.Arg857Ter
ENST00000704363.1:c.2548C>T ENSP00000515871.1:p.Arg850Ter
ENST00000687212.1:c.2638C>T MANE Select ENSP00000509890.1:p.Arg880Ter
ENST00000262811.10:c.2551C>T ENSP00000262811.4:p.Arg851Ter
NM_015016.1:c.2551C>T NP_055831.1:p.Arg851Ter
XM_005259822.2:c.3085C>T XP_005259879.2:p.Arg1029Ter
XM_005259823.2:c.2590C>T XP_005259880.1:p.Arg864Ter
XM_005259824.2:c.2572C>T XP_005259881.1:p.Arg858Ter
XM_005259825.2:c.2569C>T XP_005259882.1:p.Arg857Ter
XM_005259826.2:c.2566C>T XP_005259883.1:p.Arg856Ter
XM_005259827.1:c.2569C>T XP_005259884.1:p.Arg857Ter
XM_006722693.2:c.3109C>T XP_006722756.2:p.Arg1037Ter
XM_006722694.2:c.3106C>T XP_006722757.2:p.Arg1036Ter
XM_006722695.2:c.3088C>T XP_006722758.2:p.Arg1030Ter
XM_006722696.2:c.3109C>T XP_006722759.2:p.Arg1037Ter
XM_006722697.2:c.3088C>T XP_006722760.2:p.Arg1030Ter
XM_006722698.2:c.2326C>T XP_006722761.1:p.Arg776Ter
XM_006722699.2:c.2854C>T XP_006722762.2:p.Arg952Ter
XM_006722700.2:c.2566C>T XP_006722763.1:p.Arg856Ter
XM_011527823.1:c.2662C>T XP_011526125.1:p.Arg888Ter
XM_005259823.3:c.2590C>T XP_005259880.1:p.Arg864Ter
XM_005259826.3:c.2566C>T XP_005259883.1:p.Arg856Ter
XM_005259827.3:c.2569C>T XP_005259884.1:p.Arg857Ter
XM_006722700.3:c.2566C>T XP_006722763.1:p.Arg856Ter
XM_017026506.1:c.2851C>T XP_016881995.1:p.Arg951Ter
XM_017026507.1:c.2833C>T XP_016881996.1:p.Arg945Ter
XM_017026508.1:c.2830C>T XP_016881997.1:p.Arg944Ter
XM_017026509.1:c.2854C>T XP_016881998.1:p.Arg952Ter
XM_017026510.2:c.2833C>T XP_016881999.1:p.Arg945Ter
XM_017026511.1:c.2638C>T XP_016882000.1:p.Arg880Ter
XM_017026512.1:c.2551C>T XP_016882001.1:p.Arg851Ter
XM_017026513.1:c.2548C>T XP_016882002.1:p.Arg850Ter
XM_017026514.1:c.2326C>T XP_016882003.1:p.Arg776Ter
XM_017026515.1:c.2326C>T XP_016882004.1:p.Arg776Ter
XM_017026516.1:c.2851C>T XP_016882005.1:p.Arg951Ter
NM_015016.2:c.2551C>T NP_055831.1:p.Arg851Ter
NM_001393501.1:c.2662C>T NP_001380430.1:p.Arg888Ter
NM_001393502.1:c.2641C>T NP_001380431.1:p.Arg881Ter
NM_001393503.1:c.2638C>T NP_001380432.1:p.Arg880Ter
NM_001393504.1:c.2638C>T MANE Select NP_001380433.1:p.Arg880Ter
NM_001393505.1:c.2635C>T NP_001380434.1:p.Arg879Ter
NM_001393506.1:c.2590C>T NP_001380435.1:p.Arg864Ter
NM_001393507.1:c.2617C>T NP_001380436.1:p.Arg873Ter
NM_001393508.1:c.2572C>T NP_001380437.1:p.Arg858Ter
NM_001393509.1:c.2569C>T NP_001380438.1:p.Arg857Ter
NM_001393510.1:c.2569C>T NP_001380439.1:p.Arg857Ter
NM_001393511.1:c.2566C>T NP_001380440.1:p.Arg856Ter
NM_001393512.1:c.2569C>T NP_001380441.1:p.Arg857Ter
NM_001393513.1:c.2590C>T NP_001380442.1:p.Arg864Ter
NM_001393514.1:c.2551C>T NP_001380443.1:p.Arg851Ter
NM_001393515.1:c.2548C>T NP_001380444.1:p.Arg850Ter
NM_001393516.1:c.2572C>T NP_001380445.1:p.Arg858Ter
NM_001393517.1:c.2569C>T NP_001380446.1:p.Arg857Ter
NM_001393518.1:c.2569C>T NP_001380447.1:p.Arg857Ter
NM_001393519.1:c.2566C>T NP_001380448.1:p.Arg856Ter
NM_001393520.1:c.2548C>T NP_001380449.1:p.Arg850Ter
NM_001393521.1:c.2524C>T NP_001380450.1:p.Arg842Ter