Canonical Allele Identifier: CA359987206
Gene: MCCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71635039G>C , CM000667.2:g.71635039G>C GRCh38
NC_000005.9:g.70930866G>C , CM000667.1:g.70930866G>C GRCh37
NC_000005.8:g.70966622G>C NCBI36
NG_008882.1:g.52752G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.856G>C
ENST00000505787.8:n.2740G>C
ENST00000509358.7:c.900G>C ENSP00000420994.3:p.Leu300Phe
ENST00000509539.3:c.162G>C ENSP00000425474.3:p.Leu54Phe
ENST00000510895.7:n.1023G>C
ENST00000629193.3:c.786G>C ENSP00000486535.2:p.Leu262Phe
ENST00000681968.1:c.393G>C ENSP00000508143.1:p.Leu131Phe
ENST00000682045.1:c.756G>C ENSP00000507329.1:p.Leu252Phe
ENST00000682214.1:c.507G>C ENSP00000507336.1:p.Leu169Phe
ENST00000682499.1:n.1721G>C
ENST00000682541.1:c.900G>C ENSP00000507673.1:p.Leu300Phe
ENST00000682687.1:c.900G>C ENSP00000507945.1:p.Leu300Phe
ENST00000682727.1:c.900G>C ENSP00000507393.1:p.Leu300Phe
ENST00000682876.1:c.1029G>C ENSP00000508389.1:p.Leu343Phe
ENST00000683098.1:c.803+2854G>C ENSP00000507670.1:n.803+2854G>C
ENST00000683258.1:c.*621G>C ENSP00000507448.1:n.*621G>C
ENST00000683339.1:c.684G>C ENSP00000507758.1:p.Leu228Phe
ENST00000683403.1:c.813+87G>C ENSP00000507896.1:n.813+87G>C
ENST00000683429.1:c.507G>C ENSP00000507697.1:p.Leu169Phe
ENST00000683665.1:c.900G>C ENSP00000507068.1:p.Leu300Phe
ENST00000683789.1:c.786G>C ENSP00000507012.1:p.Leu262Phe
ENST00000683847.1:n.744G>C
ENST00000683882.1:c.900G>C ENSP00000506735.1:p.Leu300Phe
ENST00000684024.1:c.*571G>C ENSP00000507175.1:n.*571G>C
ENST00000684254.1:c.*626G>C ENSP00000508001.1:n.*626G>C
ENST00000684310.1:c.162G>C ENSP00000507550.1:p.Leu54Phe
ENST00000684530.1:c.162G>C ENSP00000507439.1:p.Leu54Phe
ENST00000684652.1:n.1902G>C
ENST00000340941.11:c.900G>C MANE Select ENSP00000343657.6:p.Leu300Phe
ENST00000340941.10:c.900G>C ENSP00000343657.6:p.Leu300Phe
ENST00000505435.3:n.251G>C
ENST00000505787.7:n.714G>C
ENST00000509358.6:c.900G>C ENSP00000420994.2:p.Leu300Phe
ENST00000509539.2:c.225G>C ENSP00000425474.2:p.Leu75Phe
ENST00000510895.6:n.514G>C
ENST00000512218.6:c.786G>C ENSP00000423202.2:p.Leu262Phe
ENST00000629193.2:c.786G>C ENSP00000486535.1:p.Leu262Phe
NM_022132.4:c.900G>C NP_071415.1:p.Leu300Phe
XM_005248567.1:c.786G>C XP_005248624.1:p.Leu262Phe
XM_011543528.1:c.900G>C XP_011541830.1:p.Leu300Phe
XM_011543529.1:c.900G>C XP_011541831.1:p.Leu300Phe
NM_001363147.1:c.786G>C NP_001350076.1:p.Leu262Phe
XM_011543529.2:c.900G>C XP_011541831.1:p.Leu300Phe
XM_017009688.1:c.900G>C XP_016865177.1:p.Leu300Phe
XR_001742172.1:n.940G>C
NM_022132.5:c.900G>C MANE Select NP_071415.1:p.Leu300Phe