Canonical Allele Identifier: CA1554397225
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71646220T= , CM000667.2:g.71646220T= GRCh38
NC_000005.9:g.70942047T= , CM000667.1:g.70942047T= GRCh37
NC_000005.8:g.70977803T= NCBI36
NG_008882.1:g.63933T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.2767T=
ENST00000505787.8:n.2990T=
ENST00000509539.3:c.485T= ENSP00000425474.3:n.485T=
ENST00000681968.1:c.652T= ENSP00000508143.1:p.Phe218=
ENST00000681991.1:n.1243T=
ENST00000682045.1:c.1015T= ENSP00000507329.1:p.Phe339=
ENST00000682214.1:c.766T= ENSP00000507336.1:p.Phe256=
ENST00000682231.1:n.177T=
ENST00000682438.1:n.3158T=
ENST00000682499.1:n.1980T=
ENST00000682541.1:c.*57T= ENSP00000507673.1:n.*57T=
ENST00000682640.1:n.863T=
ENST00000682667.1:n.1324T=
ENST00000682687.1:c.*111T= ENSP00000507945.1:n.*111T=
ENST00000682727.1:c.1150T= ENSP00000507393.1:p.Phe384=
ENST00000682876.1:c.1288T= ENSP00000508389.1:p.Phe430=
ENST00000683098.1:c.813T= ENSP00000507670.1:p.Thr271=
ENST00000683258.1:c.*880T= ENSP00000507448.1:n.*880T=
ENST00000683339.1:c.943T= ENSP00000507758.1:p.Phe315=
ENST00000683403.1:c.1069T= ENSP00000507896.1:p.Phe357=
ENST00000683429.1:c.766T= ENSP00000507697.1:p.Phe256=
ENST00000683789.1:c.1045T= ENSP00000507012.1:p.Phe349=
ENST00000683847.1:n.1329T=
ENST00000683882.1:c.*100T= ENSP00000506735.1:n.*100T=
ENST00000684024.1:c.*830T= ENSP00000507175.1:n.*830T=
ENST00000684132.1:c.87T=
ENST00000684254.1:c.*885T= ENSP00000508001.1:n.*885T=
ENST00000684310.1:c.325T= ENSP00000507550.1:p.Phe109=
ENST00000684474.1:n.795T=
ENST00000684530.1:c.335-2877T= ENSP00000507439.1:n.335-2877T=
ENST00000684686.1:n.778T=
ENST00000340941.11:c.1159T= MANE Select ENSP00000343657.6:p.Phe387=
ENST00000340941.10:c.1159T= ENSP00000343657.6:p.Phe387=
ENST00000509539.2:c.475T= ENSP00000425474.2:p.Phe159=
ENST00000512218.6:c.*111T= ENSP00000423202.2:n.*111T=
NM_022132.4:c.1159T= NP_071415.1:p.Phe387=
XM_005248567.1:c.1045T= XP_005248624.1:p.Phe349=
NM_001363147.1:c.1045T= NP_001350076.1:p.Phe349=
XR_001742172.1:n.1247T=
NM_022132.5:c.1159T= MANE Select NP_071415.1:p.Phe387=