Canonical Allele Identifier: CA1554397221
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71646219C= , CM000667.2:g.71646219C= GRCh38
NC_000005.9:g.70942046C= , CM000667.1:g.70942046C= GRCh37
NC_000005.8:g.70977802C= NCBI36
NG_008882.1:g.63932C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.2766C=
ENST00000505787.8:n.2989C=
ENST00000509539.3:c.484C= ENSP00000425474.3:n.484C=
ENST00000681968.1:c.651C= ENSP00000508143.1:p.His217=
ENST00000681991.1:n.1242C=
ENST00000682045.1:c.1014C= ENSP00000507329.1:p.His338=
ENST00000682214.1:c.765C= ENSP00000507336.1:p.His255=
ENST00000682231.1:n.176C=
ENST00000682438.1:n.3157C=
ENST00000682499.1:n.1979C=
ENST00000682541.1:c.*56C= ENSP00000507673.1:n.*56C=
ENST00000682640.1:n.862C=
ENST00000682667.1:n.1323C=
ENST00000682687.1:c.*110C= ENSP00000507945.1:n.*110C=
ENST00000682727.1:c.1149C= ENSP00000507393.1:p.His383=
ENST00000682876.1:c.1287C= ENSP00000508389.1:p.His429=
ENST00000683098.1:c.812C= ENSP00000507670.1:p.Thr271=
ENST00000683258.1:c.*879C= ENSP00000507448.1:n.*879C=
ENST00000683339.1:c.942C= ENSP00000507758.1:p.His314=
ENST00000683403.1:c.1068C= ENSP00000507896.1:p.His356=
ENST00000683429.1:c.765C= ENSP00000507697.1:p.His255=
ENST00000683789.1:c.1044C= ENSP00000507012.1:p.His348=
ENST00000683847.1:n.1328C=
ENST00000683882.1:c.*99C= ENSP00000506735.1:n.*99C=
ENST00000684024.1:c.*829C= ENSP00000507175.1:n.*829C=
ENST00000684132.1:c.86C=
ENST00000684254.1:c.*884C= ENSP00000508001.1:n.*884C=
ENST00000684310.1:c.324C= ENSP00000507550.1:p.His108=
ENST00000684474.1:n.794C=
ENST00000684530.1:c.335-2878C= ENSP00000507439.1:n.335-2878C=
ENST00000684686.1:n.777C=
ENST00000340941.11:c.1158C= MANE Select ENSP00000343657.6:p.His386=
ENST00000340941.10:c.1158C= ENSP00000343657.6:p.His386=
ENST00000509539.2:c.474C= ENSP00000425474.2:p.His158=
ENST00000512218.6:c.*110C= ENSP00000423202.2:n.*110C=
NM_022132.4:c.1158C= NP_071415.1:p.His386=
XM_005248567.1:c.1044C= XP_005248624.1:p.His348=
NM_001363147.1:c.1044C= NP_001350076.1:p.His348=
XR_001742172.1:n.1246C=
NM_022132.5:c.1158C= MANE Select NP_071415.1:p.His386=