Canonical Allele Identifier: CA1554387703
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71634965T= , CM000667.2:g.71634965T= GRCh38
NC_000005.9:g.70930792T= , CM000667.1:g.70930792T= GRCh37
NC_000005.8:g.70966548T= NCBI36
NG_008882.1:g.52678T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.782T=
ENST00000505787.8:n.2666T=
ENST00000509358.7:c.826T= ENSP00000420994.3:p.Trp276=
ENST00000509539.3:c.88T= ENSP00000425474.3:p.Trp30=
ENST00000510895.7:n.949T=
ENST00000629193.3:c.712T= ENSP00000486535.2:p.Trp238=
ENST00000681968.1:c.319T= ENSP00000508143.1:p.Trp107=
ENST00000682045.1:c.682T= ENSP00000507329.1:p.Trp228=
ENST00000682214.1:c.433T= ENSP00000507336.1:p.Trp145=
ENST00000682499.1:n.1647T=
ENST00000682541.1:c.826T= ENSP00000507673.1:p.Trp276=
ENST00000682687.1:c.826T= ENSP00000507945.1:p.Trp276=
ENST00000682727.1:c.826T= ENSP00000507393.1:p.Trp276=
ENST00000682876.1:c.955T= ENSP00000508389.1:p.Trp319=
ENST00000683098.1:c.803+2780T= ENSP00000507670.1:n.803+2780T=
ENST00000683258.1:c.*547T= ENSP00000507448.1:n.*547T=
ENST00000683339.1:c.610T= ENSP00000507758.1:p.Trp204=
ENST00000683403.1:c.813+13T= ENSP00000507896.1:n.813+13T=
ENST00000683429.1:c.433T= ENSP00000507697.1:p.Trp145=
ENST00000683665.1:c.826T= ENSP00000507068.1:p.Trp276=
ENST00000683789.1:c.712T= ENSP00000507012.1:p.Trp238=
ENST00000683847.1:n.670T=
ENST00000683882.1:c.826T= ENSP00000506735.1:p.Trp276=
ENST00000684024.1:c.*497T= ENSP00000507175.1:n.*497T=
ENST00000684254.1:c.*552T= ENSP00000508001.1:n.*552T=
ENST00000684310.1:c.88T= ENSP00000507550.1:p.Trp30=
ENST00000684530.1:c.88T= ENSP00000507439.1:p.Trp30=
ENST00000684652.1:n.1828T=
ENST00000340941.11:c.826T= MANE Select ENSP00000343657.6:p.Trp276=
ENST00000340941.10:c.826T= ENSP00000343657.6:p.Trp276=
ENST00000505435.3:n.177T=
ENST00000505787.7:n.640T=
ENST00000509358.6:c.826T= ENSP00000420994.2:p.Trp276=
ENST00000509539.2:c.151T= ENSP00000425474.2:p.Trp51=
ENST00000510895.6:n.440T=
ENST00000512218.6:c.712T= ENSP00000423202.2:p.Trp238=
ENST00000629193.2:c.712T= ENSP00000486535.1:p.Trp238=
NM_022132.4:c.826T= NP_071415.1:p.Trp276=
XM_005248567.1:c.712T= XP_005248624.1:p.Trp238=
XM_011543528.1:c.826T= XP_011541830.1:p.Trp276=
XM_011543529.1:c.826T= XP_011541831.1:p.Trp276=
NM_001363147.1:c.712T= NP_001350076.1:p.Trp238=
XM_011543529.2:c.826T= XP_011541831.1:p.Trp276=
XM_017009688.1:c.826T= XP_016865177.1:p.Trp276=
XR_001742172.1:n.866T=
NM_022132.5:c.826T= MANE Select NP_071415.1:p.Trp276=