Canonical Allele Identifier: CA1554387741
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71635060T= , CM000667.2:g.71635060T= GRCh38
NC_000005.9:g.70930887T= , CM000667.1:g.70930887T= GRCh37
NC_000005.8:g.70966643T= NCBI36
NG_008882.1:g.52773T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.859+18T=
ENST00000505787.8:n.2743+18T=
ENST00000509358.7:c.903+18T= ENSP00000420994.3:n.903+18T=
ENST00000509539.3:c.165+18T= ENSP00000425474.3:n.165+18T=
ENST00000510895.7:n.1026+18T=
ENST00000629193.3:c.789+18T= ENSP00000486535.2:n.789+18T=
ENST00000681968.1:c.396+18T= ENSP00000508143.1:n.396+18T=
ENST00000682045.1:c.759+18T= ENSP00000507329.1:n.759+18T=
ENST00000682214.1:c.510+18T= ENSP00000507336.1:n.510+18T=
ENST00000682499.1:n.1724+18T=
ENST00000682541.1:c.903+18T= ENSP00000507673.1:n.903+18T=
ENST00000682687.1:c.903+18T= ENSP00000507945.1:n.903+18T=
ENST00000682727.1:c.903+18T= ENSP00000507393.1:n.903+18T=
ENST00000682876.1:c.1032+18T= ENSP00000508389.1:n.1032+18T=
ENST00000683098.1:c.803+2875T= ENSP00000507670.1:n.803+2875T=
ENST00000683258.1:c.*624+18T= ENSP00000507448.1:n.*624+18T=
ENST00000683339.1:c.687+18T= ENSP00000507758.1:n.687+18T=
ENST00000683403.1:c.814-91T= ENSP00000507896.1:n.814-91T=
ENST00000683429.1:c.510+18T= ENSP00000507697.1:n.510+18T=
ENST00000683665.1:c.903+18T= ENSP00000507068.1:n.903+18T=
ENST00000683789.1:c.789+18T= ENSP00000507012.1:n.789+18T=
ENST00000683847.1:n.747+18T=
ENST00000683882.1:c.903+18T= ENSP00000506735.1:n.903+18T=
ENST00000684024.1:c.*574+18T= ENSP00000507175.1:n.*574+18T=
ENST00000684254.1:c.*629+18T= ENSP00000508001.1:n.*629+18T=
ENST00000684310.1:c.165+18T= ENSP00000507550.1:n.165+18T=
ENST00000684530.1:c.165+18T= ENSP00000507439.1:n.165+18T=
ENST00000684652.1:n.1905+18T=
ENST00000340941.11:c.903+18T= MANE Select ENSP00000343657.6:n.903+18T=
ENST00000340941.10:c.903+18T= ENSP00000343657.6:n.903+18T=
ENST00000505435.3:n.254+18T=
ENST00000505787.7:n.735T=
ENST00000509358.6:c.903+18T= ENSP00000420994.2:n.903+18T=
ENST00000509539.2:c.228+18T= ENSP00000425474.2:n.228+18T=
ENST00000510895.6:n.517+18T=
ENST00000512218.6:c.789+18T= ENSP00000423202.2:n.789+18T=
ENST00000629193.2:c.789+18T= ENSP00000486535.1:n.789+18T=
NM_022132.4:c.903+18T= NP_071415.1:n.903+18T=
XM_005248567.1:c.789+18T= XP_005248624.1:n.789+18T=
XM_011543528.1:c.903+18T= XP_011541830.1:n.903+18T=
XM_011543529.1:c.903+18T= XP_011541831.1:n.903+18T=
NM_001363147.1:c.789+18T= NP_001350076.1:n.789+18T=
XM_011543529.2:c.903+18T= XP_011541831.1:n.903+18T=
XM_017009688.1:c.903+18T= XP_016865177.1:n.903+18T=
XR_001742172.1:n.943+18T=
NM_022132.5:c.903+18T= MANE Select NP_071415.1:n.903+18T=