Canonical Allele Identifier: CA1554387977

Gene: MCCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635320_71635324delinsAAAGT , CM000667.2:g.71635320_71635324delinsAAAGT	GRCh38
NC_000005.9:g.70931147_70931151delinsAAAGT , CM000667.1:g.70931147_70931151delinsAAAGT	GRCh37
NC_000005.8:g.70966903_70966907delinsAAAGT	NCBI36
NG_008882.1:g.53033_53037delinsAAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.955+74_955+78delinsAAAGT
ENST00000505787.8:n.2839+74_2839+78delinsAAAGT
ENST00000509358.7:c.999+74_999+78delinsAAAGT	ENSP00000420994.3:n.999+74_999+78delinsAAAGT
ENST00000509539.3:c.261+74_261+78delinsAAAGT	ENSP00000425474.3:n.261+74_261+78delinsAAAGT
ENST00000510895.7:n.1196_1200delinsAAAGT
ENST00000629193.3:c.885+74_885+78delinsAAAGT	ENSP00000486535.2:n.885+74_885+78delinsAAAGT
ENST00000681968.1:c.492+74_492+78delinsAAAGT	ENSP00000508143.1:n.492+74_492+78delinsAAAGT
ENST00000682045.1:c.855+74_855+78delinsAAAGT	ENSP00000507329.1:n.855+74_855+78delinsAAAGT
ENST00000682214.1:c.606+74_606+78delinsAAAGT	ENSP00000507336.1:n.606+74_606+78delinsAAAGT
ENST00000682499.1:n.1820+74_1820+78delinsAAAGT
ENST00000682541.1:c.999+74_999+78delinsAAAGT	ENSP00000507673.1:n.999+74_999+78delinsAAAGT
ENST00000682687.1:c.999+74_999+78delinsAAAGT	ENSP00000507945.1:n.999+74_999+78delinsAAAGT
ENST00000682727.1:c.999+74_999+78delinsAAAGT	ENSP00000507393.1:n.999+74_999+78delinsAAAGT
ENST00000682876.1:c.1128+74_1128+78delinsAAAGT	ENSP00000508389.1:n.1128+74_1128+78delinsAAAGT
ENST00000683098.1:c.803+3135_803+3139delinsAAAGT	ENSP00000507670.1:n.803+3135_803+3139delinsAAAGT
ENST00000683258.1:c.*720+74_*720+78delinsAAAGT	ENSP00000507448.1:n.*720+74_*720+78delinsAAAGT
ENST00000683339.1:c.783+74_783+78delinsAAAGT	ENSP00000507758.1:n.783+74_783+78delinsAAAGT
ENST00000683403.1:c.909+74_909+78delinsAAAGT	ENSP00000507896.1:n.909+74_909+78delinsAAAGT
ENST00000683429.1:c.606+74_606+78delinsAAAGT	ENSP00000507697.1:n.606+74_606+78delinsAAAGT
ENST00000683665.1:c.999+74_999+78delinsAAAGT	ENSP00000507068.1:n.999+74_999+78delinsAAAGT
ENST00000683789.1:c.885+74_885+78delinsAAAGT	ENSP00000507012.1:n.885+74_885+78delinsAAAGT
ENST00000683847.1:n.843+74_843+78delinsAAAGT
ENST00000683882.1:c.999+74_999+78delinsAAAGT	ENSP00000506735.1:n.999+74_999+78delinsAAAGT
ENST00000684024.1:c.*670+74_*670+78delinsAAAGT	ENSP00000507175.1:n.*670+74_*670+78delinsAAAGT
ENST00000684254.1:c.*725+74_*725+78delinsAAAGT	ENSP00000508001.1:n.*725+74_*725+78delinsAAAGT
ENST00000684310.1:c.165+278_165+282delinsAAAGT	ENSP00000507550.1:n.165+278_165+282delinsAAAGT
ENST00000684530.1:c.261+74_261+78delinsAAAGT	ENSP00000507439.1:n.261+74_261+78delinsAAAGT
ENST00000684652.1:n.2075_2079delinsAAAGT
ENST00000340941.11:c.999+74_999+78delinsAAAGT MANE Select	ENSP00000343657.6:n.999+74_999+78delinsAAAGT
ENST00000340941.10:c.999+74_999+78delinsAAAGT	ENSP00000343657.6:n.999+74_999+78delinsAAAGT
ENST00000505435.3:n.350+74_350+78delinsAAAGT
ENST00000509358.6:c.999+74_999+78delinsAAAGT	ENSP00000420994.2:n.999+74_999+78delinsAAAGT
ENST00000509539.2:c.324+74_324+78delinsAAAGT	ENSP00000425474.2:n.324+74_324+78delinsAAAGT
ENST00000510895.6:n.687_691delinsAAAGT
ENST00000512218.6:c.885+74_885+78delinsAAAGT	ENSP00000423202.2:n.885+74_885+78delinsAAAGT
ENST00000629193.2:c.885+74_885+78delinsAAAGT	ENSP00000486535.1:n.885+74_885+78delinsAAAGT
NM_022132.4:c.999+74_999+78delinsAAAGT	NP_071415.1:n.999+74_999+78delinsAAAGT
XM_005248567.1:c.885+74_885+78delinsAAAGT	XP_005248624.1:n.885+74_885+78delinsAAAGT
XM_011543528.1:c.999+74_999+78delinsAAAGT	XP_011541830.1:n.999+74_999+78delinsAAAGT
XM_011543529.1:c.999+74_999+78delinsAAAGT	XP_011541831.1:n.999+74_999+78delinsAAAGT
NM_001363147.1:c.885+74_885+78delinsAAAGT	NP_001350076.1:n.885+74_885+78delinsAAAGT
XM_011543529.2:c.999+74_999+78delinsAAAGT	XP_011541831.1:n.999+74_999+78delinsAAAGT
XM_017009688.1:c.999+74_999+78delinsAAAGT	XP_016865177.1:n.999+74_999+78delinsAAAGT
XR_001742172.1:n.1039+74_1039+78delinsAAAGT
NM_022132.5:c.999+74_999+78delinsAAAGT MANE Select	NP_071415.1:n.999+74_999+78delinsAAAGT