Canonical Allele Identifier: CA2674165986

Gene: MCCC2

Linked Data

• gnomAD v4: 5-71635458-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635459_71635460insGA , CM000667.2:g.71635459_71635460insGA	GRCh38
NC_000005.9:g.70931286_70931287insGA , CM000667.1:g.70931286_70931287insGA	GRCh37
NC_000005.8:g.70967042_70967043insGA	NCBI36
NG_008882.1:g.53172_53173insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.955+213_955+214insGA
ENST00000505787.8:n.2839+213_2839+214insGA
ENST00000509358.7:c.999+213_999+214insGA	ENSP00000420994.3:n.999+213_999+214insGA
ENST00000509539.3:c.261+213_261+214insGA	ENSP00000425474.3:n.261+213_261+214insGA
ENST00000510895.7:n.1335_1336insGA
ENST00000629193.3:c.885+213_885+214insGA	ENSP00000486535.2:n.885+213_885+214insGA
ENST00000681968.1:c.492+213_492+214insGA	ENSP00000508143.1:n.492+213_492+214insGA
ENST00000682045.1:c.855+213_855+214insGA	ENSP00000507329.1:n.855+213_855+214insGA
ENST00000682214.1:c.606+213_606+214insGA	ENSP00000507336.1:n.606+213_606+214insGA
ENST00000682499.1:n.1820+213_1820+214insGA
ENST00000682541.1:c.999+213_999+214insGA	ENSP00000507673.1:n.999+213_999+214insGA
ENST00000682687.1:c.999+213_999+214insGA	ENSP00000507945.1:n.999+213_999+214insGA
ENST00000682727.1:c.999+213_999+214insGA	ENSP00000507393.1:n.999+213_999+214insGA
ENST00000682876.1:c.1128+213_1128+214insGA	ENSP00000508389.1:n.1128+213_1128+214insGA
ENST00000683098.1:c.803+3274_803+3275insGA	ENSP00000507670.1:n.803+3274_803+3275insGA
ENST00000683258.1:c.*720+213_*720+214insGA	ENSP00000507448.1:n.*720+213_*720+214insGA
ENST00000683339.1:c.783+213_783+214insGA	ENSP00000507758.1:n.783+213_783+214insGA
ENST00000683403.1:c.909+213_909+214insGA	ENSP00000507896.1:n.909+213_909+214insGA
ENST00000683429.1:c.606+213_606+214insGA	ENSP00000507697.1:n.606+213_606+214insGA
ENST00000683665.1:c.999+213_999+214insGA	ENSP00000507068.1:n.999+213_999+214insGA
ENST00000683789.1:c.885+213_885+214insGA	ENSP00000507012.1:n.885+213_885+214insGA
ENST00000683847.1:n.843+213_843+214insGA
ENST00000683882.1:c.999+213_999+214insGA	ENSP00000506735.1:n.999+213_999+214insGA
ENST00000684024.1:c.*670+213_*670+214insGA	ENSP00000507175.1:n.*670+213_*670+214insGA
ENST00000684254.1:c.*725+213_*725+214insGA	ENSP00000508001.1:n.*725+213_*725+214insGA
ENST00000684310.1:c.165+417_165+418insGA	ENSP00000507550.1:n.165+417_165+418insGA
ENST00000684530.1:c.261+213_261+214insGA	ENSP00000507439.1:n.261+213_261+214insGA
ENST00000684652.1:n.2214_2215insGA
ENST00000340941.11:c.999+213_999+214insGA MANE Select	ENSP00000343657.6:n.999+213_999+214insGA
ENST00000340941.10:c.999+213_999+214insGA	ENSP00000343657.6:n.999+213_999+214insGA
ENST00000505435.3:n.350+213_350+214insGA
ENST00000509358.6:c.999+213_999+214insGA	ENSP00000420994.2:n.999+213_999+214insGA
ENST00000509539.2:c.324+213_324+214insGA	ENSP00000425474.2:n.324+213_324+214insGA
ENST00000510895.6:n.826_827insGA
ENST00000512218.6:c.885+213_885+214insGA	ENSP00000423202.2:n.885+213_885+214insGA
ENST00000629193.2:c.885+213_885+214insGA	ENSP00000486535.1:n.885+213_885+214insGA
NM_022132.4:c.999+213_999+214insGA	NP_071415.1:n.999+213_999+214insGA
XM_005248567.1:c.885+213_885+214insGA	XP_005248624.1:n.885+213_885+214insGA
XM_011543528.1:c.999+213_999+214insGA	XP_011541830.1:n.999+213_999+214insGA
XM_011543529.1:c.999+213_999+214insGA	XP_011541831.1:n.999+213_999+214insGA
NM_001363147.1:c.885+213_885+214insGA	NP_001350076.1:n.885+213_885+214insGA
XM_011543529.2:c.999+213_999+214insGA	XP_011541831.1:n.999+213_999+214insGA
XM_017009688.1:c.999+213_999+214insGA	XP_016865177.1:n.999+213_999+214insGA
XR_001742172.1:n.1039+213_1039+214insGA
NM_022132.5:c.999+213_999+214insGA MANE Select	NP_071415.1:n.999+213_999+214insGA