Canonical Allele Identifier: CA119999411

Gene: MCCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71643610G>A , CM000667.2:g.71643610G>A	GRCh38
NC_000005.9:g.70939437G>A , CM000667.1:g.70939437G>A	GRCh37
NC_000005.8:g.70975193G>A	NCBI36
NG_008882.1:g.61323G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_022132.5:c.1073-209G>A MANE Select	NP_071415.1:n.1073-209G>A
ENST00000340941.11:c.1073-209G>A MANE Select	ENSP00000343657.6:n.1073-209G>A
NM_001363147.1:c.959-209G>A	NP_001350076.1:n.959-209G>A
NM_022132.4:c.1073-209G>A	NP_071415.1:n.1073-209G>A
ENST00000340941.10:c.1073-209G>A	ENSP00000343657.6:n.1073-209G>A
ENST00000505435.4:n.2681-209G>A
ENST00000505787.8:n.2904-209G>A
ENST00000509539.2:c.389-209G>A	ENSP00000425474.2:n.389-209G>A
ENST00000509539.3:c.399-209G>A	ENSP00000425474.3:n.399-209G>A
ENST00000512218.6:c.967-161G>A	ENSP00000423202.2:n.967-161G>A
ENST00000629193.2:c.967-161G>A	ENSP00000486535.1:n.967-161G>A
ENST00000681968.1:c.566-209G>A	ENSP00000508143.1:n.566-209G>A
ENST00000681991.1:n.1157-209G>A
ENST00000682045.1:c.929-209G>A	ENSP00000507329.1:n.929-209G>A
ENST00000682214.1:c.680-209G>A	ENSP00000507336.1:n.680-209G>A
ENST00000682231.1:n.91-209G>A
ENST00000682438.1:n.548G>A
ENST00000682499.1:n.1894-209G>A
ENST00000682541.1:c.1000-209G>A	ENSP00000507673.1:n.1000-209G>A
ENST00000682640.1:n.568G>A
ENST00000682667.1:n.1265-236G>A
ENST00000682687.1:c.1081-161G>A	ENSP00000507945.1:n.1081-161G>A
ENST00000682727.1:c.1064-209G>A	ENSP00000507393.1:n.1064-209G>A
ENST00000682876.1:c.1202-209G>A	ENSP00000508389.1:n.1202-209G>A
ENST00000683098.1:c.804-2601G>A	ENSP00000507670.1:n.804-2601G>A
ENST00000683258.1:c.*794-209G>A	ENSP00000507448.1:n.*794-209G>A
ENST00000683339.1:c.857-209G>A	ENSP00000507758.1:n.857-209G>A
ENST00000683403.1:c.983-209G>A	ENSP00000507896.1:n.983-209G>A
ENST00000683429.1:c.680-209G>A	ENSP00000507697.1:n.680-209G>A
ENST00000683789.1:c.959-209G>A	ENSP00000507012.1:n.959-209G>A
ENST00000683847.1:n.1195-161G>A
ENST00000683882.1:c.1073-161G>A	ENSP00000506735.1:n.1073-161G>A
ENST00000684024.1:c.*744-209G>A	ENSP00000507175.1:n.*744-209G>A
ENST00000684254.1:c.*799-209G>A	ENSP00000508001.1:n.*799-209G>A
ENST00000684310.1:c.239-209G>A	ENSP00000507550.1:n.239-209G>A
ENST00000684474.1:n.661-161G>A
ENST00000684530.1:c.334+2535G>A	ENSP00000507439.1:n.334+2535G>A
ENST00000684686.1:n.692-209G>A
XM_005248567.1:c.959-209G>A	XP_005248624.1:n.959-209G>A
XM_011543528.1:c.1073-161G>A	XP_011541830.1:n.1073-161G>A
XM_017009688.1:c.1064-161G>A	XP_016865177.1:n.1064-161G>A
XR_001742172.1:n.1113-161G>A