Canonical Allele Identifier: CA1554397211
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71646213T= , CM000667.2:g.71646213T= GRCh38
NC_000005.9:g.70942040T= , CM000667.1:g.70942040T= GRCh37
NC_000005.8:g.70977796T= NCBI36
NG_008882.1:g.63926T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.2760T=
ENST00000505787.8:n.2983T=
ENST00000509539.3:c.478T= ENSP00000425474.3:n.478T=
ENST00000681968.1:c.645T= ENSP00000508143.1:p.Gly215=
ENST00000681991.1:n.1236T=
ENST00000682045.1:c.1008T= ENSP00000507329.1:p.Gly336=
ENST00000682214.1:c.759T= ENSP00000507336.1:p.Gly253=
ENST00000682231.1:n.170T=
ENST00000682438.1:n.3151T=
ENST00000682499.1:n.1973T=
ENST00000682541.1:c.*50T= ENSP00000507673.1:n.*50T=
ENST00000682640.1:n.856T=
ENST00000682667.1:n.1317T=
ENST00000682687.1:c.*104T= ENSP00000507945.1:n.*104T=
ENST00000682727.1:c.1143T= ENSP00000507393.1:p.Gly381=
ENST00000682876.1:c.1281T= ENSP00000508389.1:p.Gly427=
ENST00000683098.1:c.806T= ENSP00000507670.1:p.Val269=
ENST00000683258.1:c.*873T= ENSP00000507448.1:n.*873T=
ENST00000683339.1:c.936T= ENSP00000507758.1:p.Gly312=
ENST00000683403.1:c.1062T= ENSP00000507896.1:p.Gly354=
ENST00000683429.1:c.759T= ENSP00000507697.1:p.Gly253=
ENST00000683789.1:c.1038T= ENSP00000507012.1:p.Gly346=
ENST00000683847.1:n.1322T=
ENST00000683882.1:c.*93T= ENSP00000506735.1:n.*93T=
ENST00000684024.1:c.*823T= ENSP00000507175.1:n.*823T=
ENST00000684132.1:c.80T=
ENST00000684254.1:c.*878T= ENSP00000508001.1:n.*878T=
ENST00000684310.1:c.318T= ENSP00000507550.1:p.Gly106=
ENST00000684474.1:n.788T=
ENST00000684530.1:c.335-2884T= ENSP00000507439.1:n.335-2884T=
ENST00000684686.1:n.771T=
ENST00000340941.11:c.1152T= MANE Select ENSP00000343657.6:p.Gly384=
ENST00000340941.10:c.1152T= ENSP00000343657.6:p.Gly384=
ENST00000509539.2:c.468T= ENSP00000425474.2:p.Gly156=
ENST00000512218.6:c.*104T= ENSP00000423202.2:n.*104T=
NM_022132.4:c.1152T= NP_071415.1:p.Gly384=
XM_005248567.1:c.1038T= XP_005248624.1:p.Gly346=
NM_001363147.1:c.1038T= NP_001350076.1:p.Gly346=
XR_001742172.1:n.1240T=
NM_022132.5:c.1152T= MANE Select NP_071415.1:p.Gly384=