Canonical Allele Identifier: CA359998410

Gene: MCCC2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71649255T>G , CM000667.2:g.71649255T>G	GRCh38
NC_000005.9:g.70945082T>G , CM000667.1:g.70945082T>G	GRCh37
NC_000005.8:g.70980838T>G	NCBI36
NG_008882.1:g.66968T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.2981+2T>G
ENST00000505787.8:n.3204+2T>G
ENST00000509539.3:c.699+2T>G	ENSP00000425474.3:n.699+2T>G
ENST00000681968.1:c.866+2T>G	ENSP00000508143.1:n.866+2T>G
ENST00000681991.1:n.1457+2T>G
ENST00000682045.1:c.1229+2T>G	ENSP00000507329.1:n.1229+2T>G
ENST00000682214.1:c.980+2T>G	ENSP00000507336.1:n.980+2T>G
ENST00000682231.1:n.391+2T>G
ENST00000682438.1:n.3372+2T>G
ENST00000682499.1:n.2194+2T>G
ENST00000682541.1:c.*271+2T>G	ENSP00000507673.1:n.*271+2T>G
ENST00000682640.1:n.1077+2T>G
ENST00000682667.1:n.1565+2T>G
ENST00000682687.1:c.*325+2T>G	ENSP00000507945.1:n.*325+2T>G
ENST00000682727.1:c.1364+2T>G	ENSP00000507393.1:n.1364+2T>G
ENST00000682876.1:c.1502+2T>G	ENSP00000508389.1:n.1502+2T>G
ENST00000683098.1:c.*61+2T>G	ENSP00000507670.1:n.*61+2T>G
ENST00000683258.1:c.*1094+2T>G	ENSP00000507448.1:n.*1094+2T>G
ENST00000683339.1:c.1157+2T>G	ENSP00000507758.1:n.1157+2T>G
ENST00000683403.1:c.1283+2T>G	ENSP00000507896.1:n.1283+2T>G
ENST00000683429.1:c.980+2T>G	ENSP00000507697.1:n.980+2T>G
ENST00000683789.1:c.1259+2T>G	ENSP00000507012.1:n.1259+2T>G
ENST00000683847.1:n.1543+2T>G
ENST00000683882.1:c.*314+2T>G	ENSP00000506735.1:n.*314+2T>G
ENST00000684024.1:c.*1044+2T>G	ENSP00000507175.1:n.*1044+2T>G
ENST00000684132.1:c.301+2T>G
ENST00000684254.1:c.*1099+2T>G	ENSP00000508001.1:n.*1099+2T>G
ENST00000684310.1:c.539+2T>G	ENSP00000507550.1:n.539+2T>G
ENST00000684316.1:n.213T>G
ENST00000684474.1:n.1009+2T>G
ENST00000684530.1:c.491+2T>G	ENSP00000507439.1:n.491+2T>G
ENST00000684686.1:n.992+2T>G
ENST00000340941.11:c.1373+2T>G MANE Select	ENSP00000343657.6:n.1373+2T>G
ENST00000340941.10:c.1373+2T>G	ENSP00000343657.6:n.1373+2T>G
ENST00000509539.2:c.689+2T>G	ENSP00000425474.2:n.689+2T>G
ENST00000512218.6:c.*325+2T>G	ENSP00000423202.2:n.*325+2T>G
NM_022132.4:c.1373+2T>G	NP_071415.1:n.1373+2T>G
XM_005248567.1:c.1259+2T>G	XP_005248624.1:n.1259+2T>G
NM_001363147.1:c.1259+2T>G	NP_001350076.1:n.1259+2T>G
XR_001742172.1:n.1461+2T>G
NM_022132.5:c.1373+2T>G MANE Select	NP_071415.1:n.1373+2T>G