Canonical Allele Identifier: CA1554387725
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71635015G= , CM000667.2:g.71635015G= GRCh38
NC_000005.9:g.70930842G= , CM000667.1:g.70930842G= GRCh37
NC_000005.8:g.70966598G= NCBI36
NG_008882.1:g.52728G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.832G=
ENST00000505787.8:n.2716G=
ENST00000509358.7:c.876G= ENSP00000420994.3:p.Arg292=
ENST00000509539.3:c.138G= ENSP00000425474.3:p.Arg46=
ENST00000510895.7:n.999G=
ENST00000629193.3:c.762G= ENSP00000486535.2:p.Arg254=
ENST00000681968.1:c.369G= ENSP00000508143.1:p.Arg123=
ENST00000682045.1:c.732G= ENSP00000507329.1:p.Arg244=
ENST00000682214.1:c.483G= ENSP00000507336.1:p.Arg161=
ENST00000682499.1:n.1697G=
ENST00000682541.1:c.876G= ENSP00000507673.1:p.Arg292=
ENST00000682687.1:c.876G= ENSP00000507945.1:p.Arg292=
ENST00000682727.1:c.876G= ENSP00000507393.1:p.Arg292=
ENST00000682876.1:c.1005G= ENSP00000508389.1:p.Arg335=
ENST00000683098.1:c.803+2830G= ENSP00000507670.1:n.803+2830G=
ENST00000683258.1:c.*597G= ENSP00000507448.1:n.*597G=
ENST00000683339.1:c.660G= ENSP00000507758.1:p.Arg220=
ENST00000683403.1:c.813+63G= ENSP00000507896.1:n.813+63G=
ENST00000683429.1:c.483G= ENSP00000507697.1:p.Arg161=
ENST00000683665.1:c.876G= ENSP00000507068.1:p.Arg292=
ENST00000683789.1:c.762G= ENSP00000507012.1:p.Arg254=
ENST00000683847.1:n.720G=
ENST00000683882.1:c.876G= ENSP00000506735.1:p.Arg292=
ENST00000684024.1:c.*547G= ENSP00000507175.1:n.*547G=
ENST00000684254.1:c.*602G= ENSP00000508001.1:n.*602G=
ENST00000684310.1:c.138G= ENSP00000507550.1:p.Arg46=
ENST00000684530.1:c.138G= ENSP00000507439.1:p.Arg46=
ENST00000684652.1:n.1878G=
ENST00000340941.11:c.876G= MANE Select ENSP00000343657.6:p.Arg292=
ENST00000340941.10:c.876G= ENSP00000343657.6:p.Arg292=
ENST00000505435.3:n.227G=
ENST00000505787.7:n.690G=
ENST00000509358.6:c.876G= ENSP00000420994.2:p.Arg292=
ENST00000509539.2:c.201G= ENSP00000425474.2:p.Arg67=
ENST00000510895.6:n.490G=
ENST00000512218.6:c.762G= ENSP00000423202.2:p.Arg254=
ENST00000629193.2:c.762G= ENSP00000486535.1:p.Arg254=
NM_022132.4:c.876G= NP_071415.1:p.Arg292=
XM_005248567.1:c.762G= XP_005248624.1:p.Arg254=
XM_011543528.1:c.876G= XP_011541830.1:p.Arg292=
XM_011543529.1:c.876G= XP_011541831.1:p.Arg292=
NM_001363147.1:c.762G= NP_001350076.1:p.Arg254=
XM_011543529.2:c.876G= XP_011541831.1:p.Arg292=
XM_017009688.1:c.876G= XP_016865177.1:p.Arg292=
XR_001742172.1:n.916G=
NM_022132.5:c.876G= MANE Select NP_071415.1:p.Arg292=