Canonical Allele Identifier: CA359986407

Gene: MCCC2

Linked Data

• COSMIC: COSM6257960
• MyVariant Identifiers: chr5:g.70930801G>T (hg19) ; chr5:g.71634974G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71634974G>T , CM000667.2:g.71634974G>T	GRCh38
NC_000005.9:g.70930801G>T , CM000667.1:g.70930801G>T	GRCh37
NC_000005.8:g.70966557G>T	NCBI36
NG_008882.1:g.52687G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.791G>T
ENST00000505787.8:n.2675G>T
ENST00000509358.7:c.835G>T	ENSP00000420994.3:p.Asp279Tyr
ENST00000509539.3:c.97G>T	ENSP00000425474.3:p.Asp33Tyr
ENST00000510895.7:n.958G>T
ENST00000629193.3:c.721G>T	ENSP00000486535.2:p.Asp241Tyr
ENST00000681968.1:c.328G>T	ENSP00000508143.1:p.Asp110Tyr
ENST00000682045.1:c.691G>T	ENSP00000507329.1:p.Asp231Tyr
ENST00000682214.1:c.442G>T	ENSP00000507336.1:p.Asp148Tyr
ENST00000682499.1:n.1656G>T
ENST00000682541.1:c.835G>T	ENSP00000507673.1:p.Asp279Tyr
ENST00000682687.1:c.835G>T	ENSP00000507945.1:p.Asp279Tyr
ENST00000682727.1:c.835G>T	ENSP00000507393.1:p.Asp279Tyr
ENST00000682876.1:c.964G>T	ENSP00000508389.1:p.Asp322Tyr
ENST00000683098.1:c.803+2789G>T	ENSP00000507670.1:n.803+2789G>T
ENST00000683258.1:c.*556G>T	ENSP00000507448.1:n.*556G>T
ENST00000683339.1:c.619G>T	ENSP00000507758.1:p.Asp207Tyr
ENST00000683403.1:c.813+22G>T	ENSP00000507896.1:n.813+22G>T
ENST00000683429.1:c.442G>T	ENSP00000507697.1:p.Asp148Tyr
ENST00000683665.1:c.835G>T	ENSP00000507068.1:p.Asp279Tyr
ENST00000683789.1:c.721G>T	ENSP00000507012.1:p.Asp241Tyr
ENST00000683847.1:n.679G>T
ENST00000683882.1:c.835G>T	ENSP00000506735.1:p.Asp279Tyr
ENST00000684024.1:c.*506G>T	ENSP00000507175.1:n.*506G>T
ENST00000684254.1:c.*561G>T	ENSP00000508001.1:n.*561G>T
ENST00000684310.1:c.97G>T	ENSP00000507550.1:p.Asp33Tyr
ENST00000684530.1:c.97G>T	ENSP00000507439.1:p.Asp33Tyr
ENST00000684652.1:n.1837G>T
ENST00000340941.11:c.835G>T MANE Select	ENSP00000343657.6:p.Asp279Tyr
ENST00000340941.10:c.835G>T	ENSP00000343657.6:p.Asp279Tyr
ENST00000505435.3:n.186G>T
ENST00000505787.7:n.649G>T
ENST00000509358.6:c.835G>T	ENSP00000420994.2:p.Asp279Tyr
ENST00000509539.2:c.160G>T	ENSP00000425474.2:p.Asp54Tyr
ENST00000510895.6:n.449G>T
ENST00000512218.6:c.721G>T	ENSP00000423202.2:p.Asp241Tyr
ENST00000629193.2:c.721G>T	ENSP00000486535.1:p.Asp241Tyr
NM_022132.4:c.835G>T	NP_071415.1:p.Asp279Tyr
XM_005248567.1:c.721G>T	XP_005248624.1:p.Asp241Tyr
XM_011543528.1:c.835G>T	XP_011541830.1:p.Asp279Tyr
XM_011543529.1:c.835G>T	XP_011541831.1:p.Asp279Tyr
NM_001363147.1:c.721G>T	NP_001350076.1:p.Asp241Tyr
XM_011543529.2:c.835G>T	XP_011541831.1:p.Asp279Tyr
XM_017009688.1:c.835G>T	XP_016865177.1:p.Asp279Tyr
XR_001742172.1:n.875G>T
NM_022132.5:c.835G>T MANE Select	NP_071415.1:p.Asp279Tyr