Canonical Allele Identifier: CA3297791

Gene: MCCC2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71602640dup , CM000667.2:g.71602640dup	GRCh38
NC_000005.9:g.70898467dup , CM000667.1:g.70898467dup	GRCh37
NC_000005.8:g.70934223dup	NCBI36
NG_008882.1:g.20353dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.581+7dup
ENST00000505787.8:n.2351+7dup
ENST00000509358.7:c.511+7dup	ENSP00000420994.3:n.511+7dup
ENST00000510895.7:n.634+7dup
ENST00000629193.3:c.511+7dup	ENSP00000486535.2:n.511+7dup
ENST00000681968.1:c.118+7dup	ENSP00000508143.1:n.118+7dup
ENST00000682045.1:c.367+7dup	ENSP00000507329.1:n.367+7dup
ENST00000682214.1:c.118+7dup	ENSP00000507336.1:n.118+7dup
ENST00000682499.1:n.1332+7dup
ENST00000682541.1:c.511+7dup	ENSP00000507673.1:n.511+7dup
ENST00000682687.1:c.511+7dup	ENSP00000507945.1:n.511+7dup
ENST00000682727.1:c.511+7dup	ENSP00000507393.1:n.511+7dup
ENST00000682876.1:c.511+7dup	ENSP00000508389.1:n.511+7dup
ENST00000683098.1:c.511+7dup	ENSP00000507670.1:n.511+7dup
ENST00000683258.1:c.*232+7dup	ENSP00000507448.1:n.*232+7dup
ENST00000683339.1:c.409+7dup	ENSP00000507758.1:n.409+7dup
ENST00000683403.1:c.511+7dup	ENSP00000507896.1:n.511+7dup
ENST00000683429.1:c.118+7dup	ENSP00000507697.1:n.118+7dup
ENST00000683665.1:c.511+7dup	ENSP00000507068.1:n.511+7dup
ENST00000683789.1:c.511+7dup	ENSP00000507012.1:n.511+7dup
ENST00000683882.1:c.511+7dup	ENSP00000506735.1:n.511+7dup
ENST00000684024.1:c.*182+7dup	ENSP00000507175.1:n.*182+7dup
ENST00000684254.1:c.*237+7dup	ENSP00000508001.1:n.*237+7dup
ENST00000340941.11:c.511+7dup MANE Select	ENSP00000343657.6:n.511+7dup
ENST00000340941.10:c.511+7dup	ENSP00000343657.6:n.511+7dup
ENST00000505787.7:n.325+7dup
ENST00000507169.5:n.444dup
ENST00000509358.6:c.511+7dup	ENSP00000420994.2:n.511+7dup
ENST00000510895.6:n.125+7dup
ENST00000512218.6:c.511+7dup	ENSP00000423202.2:n.511+7dup
ENST00000629193.2:c.511+7dup	ENSP00000486535.1:n.511+7dup
NM_022132.4:c.511+7dup	NP_071415.1:n.511+7dup
XM_005248567.1:c.511+7dup	XP_005248624.1:n.511+7dup
XM_011543528.1:c.511+7dup	XP_011541830.1:n.511+7dup
XM_011543529.1:c.511+7dup	XP_011541831.1:n.511+7dup
NM_001363147.1:c.511+7dup	NP_001350076.1:n.511+7dup
XM_011543529.2:c.511+7dup	XP_011541831.1:n.511+7dup
XM_017009688.1:c.511+7dup	XP_016865177.1:n.511+7dup
XR_001742172.1:n.551+7dup
NM_022132.5:c.511+7dup MANE Select	NP_071415.1:n.511+7dup