Canonical Allele Identifier: CA1554377473
Gene: MCCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71602586G= , CM000667.2:g.71602586G= GRCh38
NC_000005.9:g.70898413G= , CM000667.1:g.70898413G= GRCh37
NC_000005.8:g.70934169G= NCBI36
NG_008882.1:g.20299G=

Transcript Alleles

HGVS Amino-acid change
ENST00000505435.4:n.534G=
ENST00000505787.8:n.2304G=
ENST00000509358.7:c.464G= ENSP00000420994.3:p.Arg155=
ENST00000510895.7:n.587G=
ENST00000629193.3:c.464G= ENSP00000486535.2:p.Arg155=
ENST00000681968.1:c.71G= ENSP00000508143.1:p.Arg24=
ENST00000682045.1:c.320G= ENSP00000507329.1:p.Arg107=
ENST00000682214.1:c.71G= ENSP00000507336.1:p.Arg24=
ENST00000682499.1:n.1285G=
ENST00000682541.1:c.464G= ENSP00000507673.1:p.Arg155=
ENST00000682687.1:c.464G= ENSP00000507945.1:p.Arg155=
ENST00000682727.1:c.464G= ENSP00000507393.1:p.Arg155=
ENST00000682876.1:c.464G= ENSP00000508389.1:p.Arg155=
ENST00000683098.1:c.464G= ENSP00000507670.1:p.Arg155=
ENST00000683258.1:c.*185G= ENSP00000507448.1:n.*185G=
ENST00000683339.1:c.362G= ENSP00000507758.1:p.Arg121=
ENST00000683403.1:c.464G= ENSP00000507896.1:p.Arg155=
ENST00000683429.1:c.71G= ENSP00000507697.1:p.Arg24=
ENST00000683665.1:c.464G= ENSP00000507068.1:p.Arg155=
ENST00000683789.1:c.464G= ENSP00000507012.1:p.Arg155=
ENST00000683882.1:c.464G= ENSP00000506735.1:p.Arg155=
ENST00000684024.1:c.*135G= ENSP00000507175.1:n.*135G=
ENST00000684254.1:c.*190G= ENSP00000508001.1:n.*190G=
ENST00000340941.11:c.464G= MANE Select ENSP00000343657.6:p.Arg155=
ENST00000340941.10:c.464G= ENSP00000343657.6:p.Arg155=
ENST00000505787.7:n.278G=
ENST00000507169.5:n.390G=
ENST00000509358.6:c.464G= ENSP00000420994.2:p.Arg155=
ENST00000510895.6:n.78G=
ENST00000512218.6:c.464G= ENSP00000423202.2:p.Arg155=
ENST00000629193.2:c.464G= ENSP00000486535.1:p.Arg155=
NM_022132.4:c.464G= NP_071415.1:p.Arg155=
XM_005248567.1:c.464G= XP_005248624.1:p.Arg155=
XM_011543528.1:c.464G= XP_011541830.1:p.Arg155=
XM_011543529.1:c.464G= XP_011541831.1:p.Arg155=
NM_001363147.1:c.464G= NP_001350076.1:p.Arg155=
XM_011543529.2:c.464G= XP_011541831.1:p.Arg155=
XM_017009688.1:c.464G= XP_016865177.1:p.Arg155=
XR_001742172.1:n.504G=
NM_022132.5:c.464G= MANE Select NP_071415.1:p.Arg155=