Canonical Allele Identifier: CA1554387701
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71634964C= , CM000667.2:g.71634964C= GRCh38
NC_000005.9:g.70930791C= , CM000667.1:g.70930791C= GRCh37
NC_000005.8:g.70966547C= NCBI36
NG_008882.1:g.52677C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.781C=
ENST00000505787.8:n.2665C=
ENST00000509358.7:c.825C= ENSP00000420994.3:p.His275=
ENST00000509539.3:c.87C= ENSP00000425474.3:p.His29=
ENST00000510895.7:n.948C=
ENST00000629193.3:c.711C= ENSP00000486535.2:p.His237=
ENST00000681968.1:c.318C= ENSP00000508143.1:p.His106=
ENST00000682045.1:c.681C= ENSP00000507329.1:p.His227=
ENST00000682214.1:c.432C= ENSP00000507336.1:p.His144=
ENST00000682499.1:n.1646C=
ENST00000682541.1:c.825C= ENSP00000507673.1:p.His275=
ENST00000682687.1:c.825C= ENSP00000507945.1:p.His275=
ENST00000682727.1:c.825C= ENSP00000507393.1:p.His275=
ENST00000682876.1:c.954C= ENSP00000508389.1:p.His318=
ENST00000683098.1:c.803+2779C= ENSP00000507670.1:n.803+2779C=
ENST00000683258.1:c.*546C= ENSP00000507448.1:n.*546C=
ENST00000683339.1:c.609C= ENSP00000507758.1:p.His203=
ENST00000683403.1:c.813+12C= ENSP00000507896.1:n.813+12C=
ENST00000683429.1:c.432C= ENSP00000507697.1:p.His144=
ENST00000683665.1:c.825C= ENSP00000507068.1:p.His275=
ENST00000683789.1:c.711C= ENSP00000507012.1:p.His237=
ENST00000683847.1:n.669C=
ENST00000683882.1:c.825C= ENSP00000506735.1:p.His275=
ENST00000684024.1:c.*496C= ENSP00000507175.1:n.*496C=
ENST00000684254.1:c.*551C= ENSP00000508001.1:n.*551C=
ENST00000684310.1:c.87C= ENSP00000507550.1:p.His29=
ENST00000684530.1:c.87C= ENSP00000507439.1:p.His29=
ENST00000684652.1:n.1827C=
ENST00000340941.11:c.825C= MANE Select ENSP00000343657.6:p.His275=
ENST00000340941.10:c.825C= ENSP00000343657.6:p.His275=
ENST00000505435.3:n.176C=
ENST00000505787.7:n.639C=
ENST00000509358.6:c.825C= ENSP00000420994.2:p.His275=
ENST00000509539.2:c.150C= ENSP00000425474.2:p.His50=
ENST00000510895.6:n.439C=
ENST00000512218.6:c.711C= ENSP00000423202.2:p.His237=
ENST00000629193.2:c.711C= ENSP00000486535.1:p.His237=
NM_022132.4:c.825C= NP_071415.1:p.His275=
XM_005248567.1:c.711C= XP_005248624.1:p.His237=
XM_011543528.1:c.825C= XP_011541830.1:p.His275=
XM_011543529.1:c.825C= XP_011541831.1:p.His275=
NM_001363147.1:c.711C= NP_001350076.1:p.His237=
XM_011543529.2:c.825C= XP_011541831.1:p.His275=
XM_017009688.1:c.825C= XP_016865177.1:p.His275=
XR_001742172.1:n.865C=
NM_022132.5:c.825C= MANE Select NP_071415.1:p.His275=