Canonical Allele Identifier: CA1554387853
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71635206T= , CM000667.2:g.71635206T= GRCh38
NC_000005.9:g.70931033T= , CM000667.1:g.70931033T= GRCh37
NC_000005.8:g.70966789T= NCBI36
NG_008882.1:g.52919T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.915T=
ENST00000505787.8:n.2799T=
ENST00000509358.7:c.959T= ENSP00000420994.3:p.Ile320=
ENST00000509539.3:c.221T= ENSP00000425474.3:p.Ile74=
ENST00000510895.7:n.1082T=
ENST00000629193.3:c.845T= ENSP00000486535.2:p.Ile282=
ENST00000681968.1:c.452T= ENSP00000508143.1:p.Ile151=
ENST00000682045.1:c.815T= ENSP00000507329.1:p.Ile272=
ENST00000682214.1:c.566T= ENSP00000507336.1:p.Ile189=
ENST00000682499.1:n.1780T=
ENST00000682541.1:c.959T= ENSP00000507673.1:p.Ile320=
ENST00000682687.1:c.959T= ENSP00000507945.1:p.Ile320=
ENST00000682727.1:c.959T= ENSP00000507393.1:p.Ile320=
ENST00000682876.1:c.1088T= ENSP00000508389.1:p.Ile363=
ENST00000683098.1:c.803+3021T= ENSP00000507670.1:n.803+3021T=
ENST00000683258.1:c.*680T= ENSP00000507448.1:n.*680T=
ENST00000683339.1:c.743T= ENSP00000507758.1:p.Ile248=
ENST00000683403.1:c.869T= ENSP00000507896.1:p.Ile290=
ENST00000683429.1:c.566T= ENSP00000507697.1:p.Ile189=
ENST00000683665.1:c.959T= ENSP00000507068.1:p.Ile320=
ENST00000683789.1:c.845T= ENSP00000507012.1:p.Ile282=
ENST00000683847.1:n.803T=
ENST00000683882.1:c.959T= ENSP00000506735.1:p.Ile320=
ENST00000684024.1:c.*630T= ENSP00000507175.1:n.*630T=
ENST00000684254.1:c.*685T= ENSP00000508001.1:n.*685T=
ENST00000684310.1:c.165+164T= ENSP00000507550.1:n.165+164T=
ENST00000684530.1:c.221T= ENSP00000507439.1:p.Ile74=
ENST00000684652.1:n.1961T=
ENST00000340941.11:c.959T= MANE Select ENSP00000343657.6:p.Ile320=
ENST00000340941.10:c.959T= ENSP00000343657.6:p.Ile320=
ENST00000505435.3:n.310T=
ENST00000509358.6:c.959T= ENSP00000420994.2:p.Ile320=
ENST00000509539.2:c.284T= ENSP00000425474.2:p.Ile95=
ENST00000510895.6:n.573T=
ENST00000512218.6:c.845T= ENSP00000423202.2:p.Ile282=
ENST00000629193.2:c.845T= ENSP00000486535.1:p.Ile282=
NM_022132.4:c.959T= NP_071415.1:p.Ile320=
XM_005248567.1:c.845T= XP_005248624.1:p.Ile282=
XM_011543528.1:c.959T= XP_011541830.1:p.Ile320=
XM_011543529.1:c.959T= XP_011541831.1:p.Ile320=
NM_001363147.1:c.845T= NP_001350076.1:p.Ile282=
XM_011543529.2:c.959T= XP_011541831.1:p.Ile320=
XM_017009688.1:c.959T= XP_016865177.1:p.Ile320=
XR_001742172.1:n.999T=
NM_022132.5:c.959T= MANE Select NP_071415.1:p.Ile320=