Canonical Allele Identifier: CA359987657

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70931021A>C (hg19) ; chr5:g.71635194A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635194A>C , CM000667.2:g.71635194A>C	GRCh38
NC_000005.9:g.70931021A>C , CM000667.1:g.70931021A>C	GRCh37
NC_000005.8:g.70966777A>C	NCBI36
NG_008882.1:g.52907A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.903A>C
ENST00000505787.8:n.2787A>C
ENST00000509358.7:c.947A>C	ENSP00000420994.3:p.Glu316Ala
ENST00000509539.3:c.209A>C	ENSP00000425474.3:p.Glu70Ala
ENST00000510895.7:n.1070A>C
ENST00000629193.3:c.833A>C	ENSP00000486535.2:p.Glu278Ala
ENST00000681968.1:c.440A>C	ENSP00000508143.1:p.Glu147Ala
ENST00000682045.1:c.803A>C	ENSP00000507329.1:p.Glu268Ala
ENST00000682214.1:c.554A>C	ENSP00000507336.1:p.Glu185Ala
ENST00000682499.1:n.1768A>C
ENST00000682541.1:c.947A>C	ENSP00000507673.1:p.Glu316Ala
ENST00000682687.1:c.947A>C	ENSP00000507945.1:p.Glu316Ala
ENST00000682727.1:c.947A>C	ENSP00000507393.1:p.Glu316Ala
ENST00000682876.1:c.1076A>C	ENSP00000508389.1:p.Glu359Ala
ENST00000683098.1:c.803+3009A>C	ENSP00000507670.1:n.803+3009A>C
ENST00000683258.1:c.*668A>C	ENSP00000507448.1:n.*668A>C
ENST00000683339.1:c.731A>C	ENSP00000507758.1:p.Glu244Ala
ENST00000683403.1:c.857A>C	ENSP00000507896.1:p.Glu286Ala
ENST00000683429.1:c.554A>C	ENSP00000507697.1:p.Glu185Ala
ENST00000683665.1:c.947A>C	ENSP00000507068.1:p.Glu316Ala
ENST00000683789.1:c.833A>C	ENSP00000507012.1:p.Glu278Ala
ENST00000683847.1:n.791A>C
ENST00000683882.1:c.947A>C	ENSP00000506735.1:p.Glu316Ala
ENST00000684024.1:c.*618A>C	ENSP00000507175.1:n.*618A>C
ENST00000684254.1:c.*673A>C	ENSP00000508001.1:n.*673A>C
ENST00000684310.1:c.165+152A>C	ENSP00000507550.1:n.165+152A>C
ENST00000684530.1:c.209A>C	ENSP00000507439.1:p.Glu70Ala
ENST00000684652.1:n.1949A>C
ENST00000340941.11:c.947A>C MANE Select	ENSP00000343657.6:p.Glu316Ala
ENST00000340941.10:c.947A>C	ENSP00000343657.6:p.Glu316Ala
ENST00000505435.3:n.298A>C
ENST00000509358.6:c.947A>C	ENSP00000420994.2:p.Glu316Ala
ENST00000509539.2:c.272A>C	ENSP00000425474.2:p.Glu91Ala
ENST00000510895.6:n.561A>C
ENST00000512218.6:c.833A>C	ENSP00000423202.2:p.Glu278Ala
ENST00000629193.2:c.833A>C	ENSP00000486535.1:p.Glu278Ala
NM_022132.4:c.947A>C	NP_071415.1:p.Glu316Ala
XM_005248567.1:c.833A>C	XP_005248624.1:p.Glu278Ala
XM_011543528.1:c.947A>C	XP_011541830.1:p.Glu316Ala
XM_011543529.1:c.947A>C	XP_011541831.1:p.Glu316Ala
NM_001363147.1:c.833A>C	NP_001350076.1:p.Glu278Ala
XM_011543529.2:c.947A>C	XP_011541831.1:p.Glu316Ala
XM_017009688.1:c.947A>C	XP_016865177.1:p.Glu316Ala
XR_001742172.1:n.987A>C
NM_022132.5:c.947A>C MANE Select	NP_071415.1:p.Glu316Ala