Canonical Allele Identifier: CA359987410
Gene: MCCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.71635158T>G , CM000667.2:g.71635158T>G GRCh38
NC_000005.9:g.70930985T>G , CM000667.1:g.70930985T>G GRCh37
NC_000005.8:g.70966741T>G NCBI36
NG_008882.1:g.52871T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000505435.4:n.867T>G
ENST00000505787.8:n.2751T>G
ENST00000509358.7:c.911T>G ENSP00000420994.3:p.Ile304Ser
ENST00000509539.3:c.173T>G ENSP00000425474.3:p.Ile58Ser
ENST00000510895.7:n.1034T>G
ENST00000629193.3:c.797T>G ENSP00000486535.2:p.Ile266Ser
ENST00000681968.1:c.404T>G ENSP00000508143.1:p.Ile135Ser
ENST00000682045.1:c.767T>G ENSP00000507329.1:p.Ile256Ser
ENST00000682214.1:c.518T>G ENSP00000507336.1:p.Ile173Ser
ENST00000682499.1:n.1732T>G
ENST00000682541.1:c.911T>G ENSP00000507673.1:p.Ile304Ser
ENST00000682687.1:c.911T>G ENSP00000507945.1:p.Ile304Ser
ENST00000682727.1:c.911T>G ENSP00000507393.1:p.Ile304Ser
ENST00000682876.1:c.1040T>G ENSP00000508389.1:p.Ile347Ser
ENST00000683098.1:c.803+2973T>G ENSP00000507670.1:n.803+2973T>G
ENST00000683258.1:c.*632T>G ENSP00000507448.1:n.*632T>G
ENST00000683339.1:c.695T>G ENSP00000507758.1:p.Ile232Ser
ENST00000683403.1:c.821T>G ENSP00000507896.1:p.Ile274Ser
ENST00000683429.1:c.518T>G ENSP00000507697.1:p.Ile173Ser
ENST00000683665.1:c.911T>G ENSP00000507068.1:p.Ile304Ser
ENST00000683789.1:c.797T>G ENSP00000507012.1:p.Ile266Ser
ENST00000683847.1:n.755T>G
ENST00000683882.1:c.911T>G ENSP00000506735.1:p.Ile304Ser
ENST00000684024.1:c.*582T>G ENSP00000507175.1:n.*582T>G
ENST00000684254.1:c.*637T>G ENSP00000508001.1:n.*637T>G
ENST00000684310.1:c.165+116T>G ENSP00000507550.1:n.165+116T>G
ENST00000684530.1:c.173T>G ENSP00000507439.1:p.Ile58Ser
ENST00000684652.1:n.1913T>G
ENST00000340941.11:c.911T>G MANE Select ENSP00000343657.6:p.Ile304Ser
ENST00000340941.10:c.911T>G ENSP00000343657.6:p.Ile304Ser
ENST00000505435.3:n.262T>G
ENST00000509358.6:c.911T>G ENSP00000420994.2:p.Ile304Ser
ENST00000509539.2:c.236T>G ENSP00000425474.2:p.Ile79Ser
ENST00000510895.6:n.525T>G
ENST00000512218.6:c.797T>G ENSP00000423202.2:p.Ile266Ser
ENST00000629193.2:c.797T>G ENSP00000486535.1:p.Ile266Ser
NM_022132.4:c.911T>G NP_071415.1:p.Ile304Ser
XM_005248567.1:c.797T>G XP_005248624.1:p.Ile266Ser
XM_011543528.1:c.911T>G XP_011541830.1:p.Ile304Ser
XM_011543529.1:c.911T>G XP_011541831.1:p.Ile304Ser
NM_001363147.1:c.797T>G NP_001350076.1:p.Ile266Ser
XM_011543529.2:c.911T>G XP_011541831.1:p.Ile304Ser
XM_017009688.1:c.911T>G XP_016865177.1:p.Ile304Ser
XR_001742172.1:n.951T>G
NM_022132.5:c.911T>G MANE Select NP_071415.1:p.Ile304Ser