Canonical Allele Identifier: CA1554387870
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71635216T= , CM000667.2:g.71635216T= GRCh38
NC_000005.9:g.70931043T= , CM000667.1:g.70931043T= GRCh37
NC_000005.8:g.70966799T= NCBI36
NG_008882.1:g.52929T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.925T=
ENST00000505787.8:n.2809T=
ENST00000509358.7:c.969T= ENSP00000420994.3:p.Ala323=
ENST00000509539.3:c.231T= ENSP00000425474.3:p.Ala77=
ENST00000510895.7:n.1092T=
ENST00000629193.3:c.855T= ENSP00000486535.2:p.Ala285=
ENST00000681968.1:c.462T= ENSP00000508143.1:p.Ala154=
ENST00000682045.1:c.825T= ENSP00000507329.1:p.Ala275=
ENST00000682214.1:c.576T= ENSP00000507336.1:p.Ala192=
ENST00000682499.1:n.1790T=
ENST00000682541.1:c.969T= ENSP00000507673.1:p.Ala323=
ENST00000682687.1:c.969T= ENSP00000507945.1:p.Ala323=
ENST00000682727.1:c.969T= ENSP00000507393.1:p.Ala323=
ENST00000682876.1:c.1098T= ENSP00000508389.1:p.Ala366=
ENST00000683098.1:c.803+3031T= ENSP00000507670.1:n.803+3031T=
ENST00000683258.1:c.*690T= ENSP00000507448.1:n.*690T=
ENST00000683339.1:c.753T= ENSP00000507758.1:p.Ala251=
ENST00000683403.1:c.879T= ENSP00000507896.1:p.Ala293=
ENST00000683429.1:c.576T= ENSP00000507697.1:p.Ala192=
ENST00000683665.1:c.969T= ENSP00000507068.1:p.Ala323=
ENST00000683789.1:c.855T= ENSP00000507012.1:p.Ala285=
ENST00000683847.1:n.813T=
ENST00000683882.1:c.969T= ENSP00000506735.1:p.Ala323=
ENST00000684024.1:c.*640T= ENSP00000507175.1:n.*640T=
ENST00000684254.1:c.*695T= ENSP00000508001.1:n.*695T=
ENST00000684310.1:c.165+174T= ENSP00000507550.1:n.165+174T=
ENST00000684530.1:c.231T= ENSP00000507439.1:p.Ala77=
ENST00000684652.1:n.1971T=
ENST00000340941.11:c.969T= MANE Select ENSP00000343657.6:p.Ala323=
ENST00000340941.10:c.969T= ENSP00000343657.6:p.Ala323=
ENST00000505435.3:n.320T=
ENST00000509358.6:c.969T= ENSP00000420994.2:p.Ala323=
ENST00000509539.2:c.294T= ENSP00000425474.2:p.Ala98=
ENST00000510895.6:n.583T=
ENST00000512218.6:c.855T= ENSP00000423202.2:p.Ala285=
ENST00000629193.2:c.855T= ENSP00000486535.1:p.Ala285=
NM_022132.4:c.969T= NP_071415.1:p.Ala323=
XM_005248567.1:c.855T= XP_005248624.1:p.Ala285=
XM_011543528.1:c.969T= XP_011541830.1:p.Ala323=
XM_011543529.1:c.969T= XP_011541831.1:p.Ala323=
NM_001363147.1:c.855T= NP_001350076.1:p.Ala285=
XM_011543529.2:c.969T= XP_011541831.1:p.Ala323=
XM_017009688.1:c.969T= XP_016865177.1:p.Ala323=
XR_001742172.1:n.1009T=
NM_022132.5:c.969T= MANE Select NP_071415.1:p.Ala323=