Canonical Allele Identifier: CA1554387898
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71635240C= , CM000667.2:g.71635240C= GRCh38
NC_000005.9:g.70931067C= , CM000667.1:g.70931067C= GRCh37
NC_000005.8:g.70966823C= NCBI36
NG_008882.1:g.52953C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.949C=
ENST00000505787.8:n.2833C=
ENST00000509358.7:c.993C= ENSP00000420994.3:p.Val331=
ENST00000509539.3:c.255C= ENSP00000425474.3:p.Val85=
ENST00000510895.7:n.1116C=
ENST00000629193.3:c.879C= ENSP00000486535.2:p.Val293=
ENST00000681968.1:c.486C= ENSP00000508143.1:p.Val162=
ENST00000682045.1:c.849C= ENSP00000507329.1:p.Val283=
ENST00000682214.1:c.600C= ENSP00000507336.1:p.Val200=
ENST00000682499.1:n.1814C=
ENST00000682541.1:c.993C= ENSP00000507673.1:p.Val331=
ENST00000682687.1:c.993C= ENSP00000507945.1:p.Val331=
ENST00000682727.1:c.993C= ENSP00000507393.1:p.Val331=
ENST00000682876.1:c.1122C= ENSP00000508389.1:p.Val374=
ENST00000683098.1:c.803+3055C= ENSP00000507670.1:n.803+3055C=
ENST00000683258.1:c.*714C= ENSP00000507448.1:n.*714C=
ENST00000683339.1:c.777C= ENSP00000507758.1:p.Val259=
ENST00000683403.1:c.903C= ENSP00000507896.1:p.Val301=
ENST00000683429.1:c.600C= ENSP00000507697.1:p.Val200=
ENST00000683665.1:c.993C= ENSP00000507068.1:p.Val331=
ENST00000683789.1:c.879C= ENSP00000507012.1:p.Val293=
ENST00000683847.1:n.837C=
ENST00000683882.1:c.993C= ENSP00000506735.1:p.Val331=
ENST00000684024.1:c.*664C= ENSP00000507175.1:n.*664C=
ENST00000684254.1:c.*719C= ENSP00000508001.1:n.*719C=
ENST00000684310.1:c.165+198C= ENSP00000507550.1:n.165+198C=
ENST00000684530.1:c.255C= ENSP00000507439.1:p.Val85=
ENST00000684652.1:n.1995C=
ENST00000340941.11:c.993C= MANE Select ENSP00000343657.6:p.Val331=
ENST00000340941.10:c.993C= ENSP00000343657.6:p.Val331=
ENST00000505435.3:n.344C=
ENST00000509358.6:c.993C= ENSP00000420994.2:p.Val331=
ENST00000509539.2:c.318C= ENSP00000425474.2:p.Val106=
ENST00000510895.6:n.607C=
ENST00000512218.6:c.879C= ENSP00000423202.2:p.Val293=
ENST00000629193.2:c.879C= ENSP00000486535.1:p.Val293=
NM_022132.4:c.993C= NP_071415.1:p.Val331=
XM_005248567.1:c.879C= XP_005248624.1:p.Val293=
XM_011543528.1:c.993C= XP_011541830.1:p.Val331=
XM_011543529.1:c.993C= XP_011541831.1:p.Val331=
NM_001363147.1:c.879C= NP_001350076.1:p.Val293=
XM_011543529.2:c.993C= XP_011541831.1:p.Val331=
XM_017009688.1:c.993C= XP_016865177.1:p.Val331=
XR_001742172.1:n.1033C=
NM_022132.5:c.993C= MANE Select NP_071415.1:p.Val331=