Canonical Allele Identifier: CA359986193
Gene: MCCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71634956A>T , CM000667.2:g.71634956A>T GRCh38
NC_000005.9:g.70930783A>T , CM000667.1:g.70930783A>T GRCh37
NC_000005.8:g.70966539A>T NCBI36
NG_008882.1:g.52669A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.773A>T
ENST00000505787.8:n.2657A>T
ENST00000509358.7:c.817A>T ENSP00000420994.3:p.Ser273Cys
ENST00000509539.3:c.79A>T ENSP00000425474.3:p.Ser27Cys
ENST00000510895.7:n.940A>T
ENST00000629193.3:c.703A>T ENSP00000486535.2:p.Ser235Cys
ENST00000681968.1:c.310A>T ENSP00000508143.1:p.Ser104Cys
ENST00000682045.1:c.673A>T ENSP00000507329.1:p.Ser225Cys
ENST00000682214.1:c.424A>T ENSP00000507336.1:p.Ser142Cys
ENST00000682499.1:n.1638A>T
ENST00000682541.1:c.817A>T ENSP00000507673.1:p.Ser273Cys
ENST00000682687.1:c.817A>T ENSP00000507945.1:p.Ser273Cys
ENST00000682727.1:c.817A>T ENSP00000507393.1:p.Ser273Cys
ENST00000682876.1:c.946A>T ENSP00000508389.1:p.Ser316Cys
ENST00000683098.1:c.803+2771A>T ENSP00000507670.1:n.803+2771A>T
ENST00000683258.1:c.*538A>T ENSP00000507448.1:n.*538A>T
ENST00000683339.1:c.601A>T ENSP00000507758.1:p.Ser201Cys
ENST00000683403.1:c.813+4A>T ENSP00000507896.1:n.813+4A>T
ENST00000683429.1:c.424A>T ENSP00000507697.1:p.Ser142Cys
ENST00000683665.1:c.817A>T ENSP00000507068.1:p.Ser273Cys
ENST00000683789.1:c.703A>T ENSP00000507012.1:p.Ser235Cys
ENST00000683847.1:n.661A>T
ENST00000683882.1:c.817A>T ENSP00000506735.1:p.Ser273Cys
ENST00000684024.1:c.*488A>T ENSP00000507175.1:n.*488A>T
ENST00000684254.1:c.*543A>T ENSP00000508001.1:n.*543A>T
ENST00000684310.1:c.79A>T ENSP00000507550.1:p.Ser27Cys
ENST00000684530.1:c.79A>T ENSP00000507439.1:p.Ser27Cys
ENST00000684652.1:n.1819A>T
ENST00000340941.11:c.817A>T MANE Select ENSP00000343657.6:p.Ser273Cys
ENST00000340941.10:c.817A>T ENSP00000343657.6:p.Ser273Cys
ENST00000505435.3:n.168A>T
ENST00000505787.7:n.631A>T
ENST00000509358.6:c.817A>T ENSP00000420994.2:p.Ser273Cys
ENST00000509539.2:c.142A>T ENSP00000425474.2:p.Ser48Cys
ENST00000510895.6:n.431A>T
ENST00000512218.6:c.703A>T ENSP00000423202.2:p.Ser235Cys
ENST00000629193.2:c.703A>T ENSP00000486535.1:p.Ser235Cys
NM_022132.4:c.817A>T NP_071415.1:p.Ser273Cys
XM_005248567.1:c.703A>T XP_005248624.1:p.Ser235Cys
XM_011543528.1:c.817A>T XP_011541830.1:p.Ser273Cys
XM_011543529.1:c.817A>T XP_011541831.1:p.Ser273Cys
NM_001363147.1:c.703A>T NP_001350076.1:p.Ser235Cys
XM_011543529.2:c.817A>T XP_011541831.1:p.Ser273Cys
XM_017009688.1:c.817A>T XP_016865177.1:p.Ser273Cys
XR_001742172.1:n.857A>T
NM_022132.5:c.817A>T MANE Select NP_071415.1:p.Ser273Cys