Canonical Allele Identifier: CA359986049

Gene: MCCC2

Linked Data

• MyVariant Identifiers: chr5:g.70930773G>C (hg19) ; chr5:g.71634946G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71634946G>C , CM000667.2:g.71634946G>C	GRCh38
NC_000005.9:g.70930773G>C , CM000667.1:g.70930773G>C	GRCh37
NC_000005.8:g.70966529G>C	NCBI36
NG_008882.1:g.52659G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.763G>C
ENST00000505787.8:n.2647G>C
ENST00000509358.7:c.807G>C	ENSP00000420994.3:p.Lys269Asn
ENST00000509539.3:c.69G>C	ENSP00000425474.3:p.Lys23Asn
ENST00000510895.7:n.930G>C
ENST00000629193.3:c.693G>C	ENSP00000486535.2:p.Lys231Asn
ENST00000681968.1:c.300G>C	ENSP00000508143.1:p.Lys100Asn
ENST00000682045.1:c.663G>C	ENSP00000507329.1:p.Lys221Asn
ENST00000682214.1:c.414G>C	ENSP00000507336.1:p.Lys138Asn
ENST00000682499.1:n.1628G>C
ENST00000682541.1:c.807G>C	ENSP00000507673.1:p.Lys269Asn
ENST00000682687.1:c.807G>C	ENSP00000507945.1:p.Lys269Asn
ENST00000682727.1:c.807G>C	ENSP00000507393.1:p.Lys269Asn
ENST00000682876.1:c.936G>C	ENSP00000508389.1:p.Lys312Asn
ENST00000683098.1:c.803+2761G>C	ENSP00000507670.1:n.803+2761G>C
ENST00000683258.1:c.*528G>C	ENSP00000507448.1:n.*528G>C
ENST00000683339.1:c.591G>C	ENSP00000507758.1:p.Lys197Asn
ENST00000683403.1:c.807G>C	ENSP00000507896.1:p.Lys269Asn
ENST00000683429.1:c.414G>C	ENSP00000507697.1:p.Lys138Asn
ENST00000683665.1:c.807G>C	ENSP00000507068.1:p.Lys269Asn
ENST00000683789.1:c.693G>C	ENSP00000507012.1:p.Lys231Asn
ENST00000683847.1:n.651G>C
ENST00000683882.1:c.807G>C	ENSP00000506735.1:p.Lys269Asn
ENST00000684024.1:c.*478G>C	ENSP00000507175.1:n.*478G>C
ENST00000684254.1:c.*533G>C	ENSP00000508001.1:n.*533G>C
ENST00000684310.1:c.69G>C	ENSP00000507550.1:p.Lys23Asn
ENST00000684530.1:c.69G>C	ENSP00000507439.1:p.Lys23Asn
ENST00000684652.1:n.1809G>C
ENST00000340941.11:c.807G>C MANE Select	ENSP00000343657.6:p.Lys269Asn
ENST00000340941.10:c.807G>C	ENSP00000343657.6:p.Lys269Asn
ENST00000505435.3:n.158G>C
ENST00000505787.7:n.621G>C
ENST00000509358.6:c.807G>C	ENSP00000420994.2:p.Lys269Asn
ENST00000509539.2:c.132G>C	ENSP00000425474.2:p.Lys44Asn
ENST00000510895.6:n.421G>C
ENST00000512218.6:c.693G>C	ENSP00000423202.2:p.Lys231Asn
ENST00000629193.2:c.693G>C	ENSP00000486535.1:p.Lys231Asn
NM_022132.4:c.807G>C	NP_071415.1:p.Lys269Asn
XM_005248567.1:c.693G>C	XP_005248624.1:p.Lys231Asn
XM_011543528.1:c.807G>C	XP_011541830.1:p.Lys269Asn
XM_011543529.1:c.807G>C	XP_011541831.1:p.Lys269Asn
NM_001363147.1:c.693G>C	NP_001350076.1:p.Lys231Asn
XM_011543529.2:c.807G>C	XP_011541831.1:p.Lys269Asn
XM_017009688.1:c.807G>C	XP_016865177.1:p.Lys269Asn
XR_001742172.1:n.847G>C
NM_022132.5:c.807G>C MANE Select	NP_071415.1:p.Lys269Asn