Canonical Allele Identifier: CA359987498

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70930997A>T (hg19) ; chr5:g.71635170A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635170A>T , CM000667.2:g.71635170A>T	GRCh38
NC_000005.9:g.70930997A>T , CM000667.1:g.70930997A>T	GRCh37
NC_000005.8:g.70966753A>T	NCBI36
NG_008882.1:g.52883A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.879A>T
ENST00000505787.8:n.2763A>T
ENST00000509358.7:c.923A>T	ENSP00000420994.3:p.Glu308Val
ENST00000509539.3:c.185A>T	ENSP00000425474.3:p.Glu62Val
ENST00000510895.7:n.1046A>T
ENST00000629193.3:c.809A>T	ENSP00000486535.2:p.Glu270Val
ENST00000681968.1:c.416A>T	ENSP00000508143.1:p.Glu139Val
ENST00000682045.1:c.779A>T	ENSP00000507329.1:p.Glu260Val
ENST00000682214.1:c.530A>T	ENSP00000507336.1:p.Glu177Val
ENST00000682499.1:n.1744A>T
ENST00000682541.1:c.923A>T	ENSP00000507673.1:p.Glu308Val
ENST00000682687.1:c.923A>T	ENSP00000507945.1:p.Glu308Val
ENST00000682727.1:c.923A>T	ENSP00000507393.1:p.Glu308Val
ENST00000682876.1:c.1052A>T	ENSP00000508389.1:p.Glu351Val
ENST00000683098.1:c.803+2985A>T	ENSP00000507670.1:n.803+2985A>T
ENST00000683258.1:c.*644A>T	ENSP00000507448.1:n.*644A>T
ENST00000683339.1:c.707A>T	ENSP00000507758.1:p.Glu236Val
ENST00000683403.1:c.833A>T	ENSP00000507896.1:p.Glu278Val
ENST00000683429.1:c.530A>T	ENSP00000507697.1:p.Glu177Val
ENST00000683665.1:c.923A>T	ENSP00000507068.1:p.Glu308Val
ENST00000683789.1:c.809A>T	ENSP00000507012.1:p.Glu270Val
ENST00000683847.1:n.767A>T
ENST00000683882.1:c.923A>T	ENSP00000506735.1:p.Glu308Val
ENST00000684024.1:c.*594A>T	ENSP00000507175.1:n.*594A>T
ENST00000684254.1:c.*649A>T	ENSP00000508001.1:n.*649A>T
ENST00000684310.1:c.165+128A>T	ENSP00000507550.1:n.165+128A>T
ENST00000684530.1:c.185A>T	ENSP00000507439.1:p.Glu62Val
ENST00000684652.1:n.1925A>T
ENST00000340941.11:c.923A>T MANE Select	ENSP00000343657.6:p.Glu308Val
ENST00000340941.10:c.923A>T	ENSP00000343657.6:p.Glu308Val
ENST00000505435.3:n.274A>T
ENST00000509358.6:c.923A>T	ENSP00000420994.2:p.Glu308Val
ENST00000509539.2:c.248A>T	ENSP00000425474.2:p.Glu83Val
ENST00000510895.6:n.537A>T
ENST00000512218.6:c.809A>T	ENSP00000423202.2:p.Glu270Val
ENST00000629193.2:c.809A>T	ENSP00000486535.1:p.Glu270Val
NM_022132.4:c.923A>T	NP_071415.1:p.Glu308Val
XM_005248567.1:c.809A>T	XP_005248624.1:p.Glu270Val
XM_011543528.1:c.923A>T	XP_011541830.1:p.Glu308Val
XM_011543529.1:c.923A>T	XP_011541831.1:p.Glu308Val
NM_001363147.1:c.809A>T	NP_001350076.1:p.Glu270Val
XM_011543529.2:c.923A>T	XP_011541831.1:p.Glu308Val
XM_017009688.1:c.923A>T	XP_016865177.1:p.Glu308Val
XR_001742172.1:n.963A>T
NM_022132.5:c.923A>T MANE Select	NP_071415.1:p.Glu308Val