Canonical Allele Identifier: CA1554388096

Gene: MCCC2

Linked Data

• dbSNP Id: rs1746883887

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635457_71635468del , CM000667.2:g.71635457_71635468del	GRCh38
NC_000005.9:g.70931284_70931295del , CM000667.1:g.70931284_70931295del	GRCh37
NC_000005.8:g.70967040_70967051del	NCBI36
NG_008882.1:g.53170_53181del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.955+211_955+222del
ENST00000505787.8:n.2839+211_2839+222del
ENST00000509358.7:c.999+211_999+222del	ENSP00000420994.3:n.999+211_999+222del
ENST00000509539.3:c.261+211_261+222del	ENSP00000425474.3:n.261+211_261+222del
ENST00000510895.7:n.1333_1344del
ENST00000629193.3:c.885+211_885+222del	ENSP00000486535.2:n.885+211_885+222del
ENST00000681968.1:c.492+211_492+222del	ENSP00000508143.1:n.492+211_492+222del
ENST00000682045.1:c.855+211_855+222del	ENSP00000507329.1:n.855+211_855+222del
ENST00000682214.1:c.606+211_606+222del	ENSP00000507336.1:n.606+211_606+222del
ENST00000682499.1:n.1820+211_1820+222del
ENST00000682541.1:c.999+211_999+222del	ENSP00000507673.1:n.999+211_999+222del
ENST00000682687.1:c.999+211_999+222del	ENSP00000507945.1:n.999+211_999+222del
ENST00000682727.1:c.999+211_999+222del	ENSP00000507393.1:n.999+211_999+222del
ENST00000682876.1:c.1128+211_1128+222del	ENSP00000508389.1:n.1128+211_1128+222del
ENST00000683098.1:c.803+3272_803+3283del	ENSP00000507670.1:n.803+3272_803+3283del
ENST00000683258.1:c.*720+211_*720+222del	ENSP00000507448.1:n.*720+211_*720+222del
ENST00000683339.1:c.783+211_783+222del	ENSP00000507758.1:n.783+211_783+222del
ENST00000683403.1:c.909+211_909+222del	ENSP00000507896.1:n.909+211_909+222del
ENST00000683429.1:c.606+211_606+222del	ENSP00000507697.1:n.606+211_606+222del
ENST00000683665.1:c.999+211_999+222del	ENSP00000507068.1:n.999+211_999+222del
ENST00000683789.1:c.885+211_885+222del	ENSP00000507012.1:n.885+211_885+222del
ENST00000683847.1:n.843+211_843+222del
ENST00000683882.1:c.999+211_999+222del	ENSP00000506735.1:n.999+211_999+222del
ENST00000684024.1:c.*670+211_*670+222del	ENSP00000507175.1:n.*670+211_*670+222del
ENST00000684254.1:c.*725+211_*725+222del	ENSP00000508001.1:n.*725+211_*725+222del
ENST00000684310.1:c.165+415_165+426del	ENSP00000507550.1:n.165+415_165+426del
ENST00000684530.1:c.261+211_261+222del	ENSP00000507439.1:n.261+211_261+222del
ENST00000684652.1:n.2212_2223del
ENST00000340941.11:c.999+211_999+222del MANE Select	ENSP00000343657.6:n.999+211_999+222del
ENST00000340941.10:c.999+211_999+222del	ENSP00000343657.6:n.999+211_999+222del
ENST00000505435.3:n.350+211_350+222del
ENST00000509358.6:c.999+211_999+222del	ENSP00000420994.2:n.999+211_999+222del
ENST00000509539.2:c.324+211_324+222del	ENSP00000425474.2:n.324+211_324+222del
ENST00000510895.6:n.824_835del
ENST00000512218.6:c.885+211_885+222del	ENSP00000423202.2:n.885+211_885+222del
ENST00000629193.2:c.885+211_885+222del	ENSP00000486535.1:n.885+211_885+222del
NM_022132.4:c.999+211_999+222del	NP_071415.1:n.999+211_999+222del
XM_005248567.1:c.885+211_885+222del	XP_005248624.1:n.885+211_885+222del
XM_011543528.1:c.999+211_999+222del	XP_011541830.1:n.999+211_999+222del
XM_011543529.1:c.999+211_999+222del	XP_011541831.1:n.999+211_999+222del
NM_001363147.1:c.885+211_885+222del	NP_001350076.1:n.885+211_885+222del
XM_011543529.2:c.999+211_999+222del	XP_011541831.1:n.999+211_999+222del
XM_017009688.1:c.999+211_999+222del	XP_016865177.1:n.999+211_999+222del
XR_001742172.1:n.1039+211_1039+222del
NM_022132.5:c.999+211_999+222del MANE Select	NP_071415.1:n.999+211_999+222del