Canonical Allele Identifier: CA119999878

Gene: MCCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71644070_71644071dup , CM000667.2:g.71644070_71644071dup	GRCh38
NC_000005.9:g.70939897_70939898dup , CM000667.1:g.70939897_70939898dup	GRCh37
NC_000005.8:g.70975653_70975654dup	NCBI36
NG_008882.1:g.61783_61784dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.2757+175_2757+176dup
ENST00000505787.8:n.2980+175_2980+176dup
ENST00000509539.3:c.475+175_475+176dup	ENSP00000425474.3:n.475+175_475+176dup
ENST00000681968.1:c.642+175_642+176dup	ENSP00000508143.1:n.642+175_642+176dup
ENST00000681991.1:n.1233+175_1233+176dup
ENST00000682045.1:c.1005+175_1005+176dup	ENSP00000507329.1:n.1005+175_1005+176dup
ENST00000682214.1:c.756+175_756+176dup	ENSP00000507336.1:n.756+175_756+176dup
ENST00000682231.1:n.167+175_167+176dup
ENST00000682438.1:n.1008_1009dup
ENST00000682499.1:n.1970+175_1970+176dup
ENST00000682541.1:c.*47+175_*47+176dup	ENSP00000507673.1:n.*47+175_*47+176dup
ENST00000682640.1:n.853+175_853+176dup
ENST00000682667.1:n.1314+175_1314+176dup
ENST00000682687.1:c.*101+175_*101+176dup	ENSP00000507945.1:n.*101+175_*101+176dup
ENST00000682727.1:c.1140+175_1140+176dup	ENSP00000507393.1:n.1140+175_1140+176dup
ENST00000682876.1:c.1278+175_1278+176dup	ENSP00000508389.1:n.1278+175_1278+176dup
ENST00000683098.1:c.804-2141_804-2140dup	ENSP00000507670.1:n.804-2141_804-2140dup
ENST00000683258.1:c.*870+175_*870+176dup	ENSP00000507448.1:n.*870+175_*870+176dup
ENST00000683339.1:c.933+175_933+176dup	ENSP00000507758.1:n.933+175_933+176dup
ENST00000683403.1:c.1059+175_1059+176dup	ENSP00000507896.1:n.1059+175_1059+176dup
ENST00000683429.1:c.756+175_756+176dup	ENSP00000507697.1:n.756+175_756+176dup
ENST00000683789.1:c.1035+175_1035+176dup	ENSP00000507012.1:n.1035+175_1035+176dup
ENST00000683847.1:n.1319+175_1319+176dup
ENST00000683882.1:c.*90+175_*90+176dup	ENSP00000506735.1:n.*90+175_*90+176dup
ENST00000684024.1:c.*820+175_*820+176dup	ENSP00000507175.1:n.*820+175_*820+176dup
ENST00000684132.1:c.77+175_77+176dup
ENST00000684254.1:c.*875+175_*875+176dup	ENSP00000508001.1:n.*875+175_*875+176dup
ENST00000684310.1:c.315+175_315+176dup	ENSP00000507550.1:n.315+175_315+176dup
ENST00000684474.1:n.785+175_785+176dup
ENST00000684530.1:c.334+2995_334+2996dup	ENSP00000507439.1:n.334+2995_334+2996dup
ENST00000684686.1:n.768+175_768+176dup
ENST00000340941.11:c.1149+175_1149+176dup MANE Select	ENSP00000343657.6:n.1149+175_1149+176dup
ENST00000340941.10:c.1149+175_1149+176dup	ENSP00000343657.6:n.1149+175_1149+176dup
ENST00000509539.2:c.465+175_465+176dup	ENSP00000425474.2:n.465+175_465+176dup
ENST00000512218.6:c.*101+175_*101+176dup	ENSP00000423202.2:n.*101+175_*101+176dup
NM_022132.4:c.1149+175_1149+176dup	NP_071415.1:n.1149+175_1149+176dup
XM_005248567.1:c.1035+175_1035+176dup	XP_005248624.1:n.1035+175_1035+176dup
NM_001363147.1:c.1035+175_1035+176dup	NP_001350076.1:n.1035+175_1035+176dup
XR_001742172.1:n.1237+175_1237+176dup
NM_022132.5:c.1149+175_1149+176dup MANE Select	NP_071415.1:n.1149+175_1149+176dup