Canonical Allele Identifier: CA359986809

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70930830G>C (hg19) ; chr5:g.71635003G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635003G>C , CM000667.2:g.71635003G>C	GRCh38
NC_000005.9:g.70930830G>C , CM000667.1:g.70930830G>C	GRCh37
NC_000005.8:g.70966586G>C	NCBI36
NG_008882.1:g.52716G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.820G>C
ENST00000505787.8:n.2704G>C
ENST00000509358.7:c.864G>C	ENSP00000420994.3:p.Arg288Ser
ENST00000509539.3:c.126G>C	ENSP00000425474.3:p.Arg42Ser
ENST00000510895.7:n.987G>C
ENST00000629193.3:c.750G>C	ENSP00000486535.2:p.Arg250Ser
ENST00000681968.1:c.357G>C	ENSP00000508143.1:p.Arg119Ser
ENST00000682045.1:c.720G>C	ENSP00000507329.1:p.Arg240Ser
ENST00000682214.1:c.471G>C	ENSP00000507336.1:p.Arg157Ser
ENST00000682499.1:n.1685G>C
ENST00000682541.1:c.864G>C	ENSP00000507673.1:p.Arg288Ser
ENST00000682687.1:c.864G>C	ENSP00000507945.1:p.Arg288Ser
ENST00000682727.1:c.864G>C	ENSP00000507393.1:p.Arg288Ser
ENST00000682876.1:c.993G>C	ENSP00000508389.1:p.Arg331Ser
ENST00000683098.1:c.803+2818G>C	ENSP00000507670.1:n.803+2818G>C
ENST00000683258.1:c.*585G>C	ENSP00000507448.1:n.*585G>C
ENST00000683339.1:c.648G>C	ENSP00000507758.1:p.Arg216Ser
ENST00000683403.1:c.813+51G>C	ENSP00000507896.1:n.813+51G>C
ENST00000683429.1:c.471G>C	ENSP00000507697.1:p.Arg157Ser
ENST00000683665.1:c.864G>C	ENSP00000507068.1:p.Arg288Ser
ENST00000683789.1:c.750G>C	ENSP00000507012.1:p.Arg250Ser
ENST00000683847.1:n.708G>C
ENST00000683882.1:c.864G>C	ENSP00000506735.1:p.Arg288Ser
ENST00000684024.1:c.*535G>C	ENSP00000507175.1:n.*535G>C
ENST00000684254.1:c.*590G>C	ENSP00000508001.1:n.*590G>C
ENST00000684310.1:c.126G>C	ENSP00000507550.1:p.Arg42Ser
ENST00000684530.1:c.126G>C	ENSP00000507439.1:p.Arg42Ser
ENST00000684652.1:n.1866G>C
ENST00000340941.11:c.864G>C MANE Select	ENSP00000343657.6:p.Arg288Ser
ENST00000340941.10:c.864G>C	ENSP00000343657.6:p.Arg288Ser
ENST00000505435.3:n.215G>C
ENST00000505787.7:n.678G>C
ENST00000509358.6:c.864G>C	ENSP00000420994.2:p.Arg288Ser
ENST00000509539.2:c.189G>C	ENSP00000425474.2:p.Arg63Ser
ENST00000510895.6:n.478G>C
ENST00000512218.6:c.750G>C	ENSP00000423202.2:p.Arg250Ser
ENST00000629193.2:c.750G>C	ENSP00000486535.1:p.Arg250Ser
NM_022132.4:c.864G>C	NP_071415.1:p.Arg288Ser
XM_005248567.1:c.750G>C	XP_005248624.1:p.Arg250Ser
XM_011543528.1:c.864G>C	XP_011541830.1:p.Arg288Ser
XM_011543529.1:c.864G>C	XP_011541831.1:p.Arg288Ser
NM_001363147.1:c.750G>C	NP_001350076.1:p.Arg250Ser
XM_011543529.2:c.864G>C	XP_011541831.1:p.Arg288Ser
XM_017009688.1:c.864G>C	XP_016865177.1:p.Arg288Ser
XR_001742172.1:n.904G>C
NM_022132.5:c.864G>C MANE Select	NP_071415.1:p.Arg288Ser