Canonical Allele Identifier: CA1554387752

Gene: MCCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71635079_71635080delinsGA , CM000667.2:g.71635079_71635080delinsGA	GRCh38
NC_000005.9:g.70930906_70930907delinsGA , CM000667.1:g.70930906_70930907delinsGA	GRCh37
NC_000005.8:g.70966662_70966663delinsGA	NCBI36
NG_008882.1:g.52792_52793delinsGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000505435.4:n.859+37_859+38delinsGA
ENST00000505787.8:n.2743+37_2743+38delinsGA
ENST00000509358.7:c.903+37_903+38delinsGA	ENSP00000420994.3:n.903+37_903+38delinsGA...
ENST00000509539.3:c.165+37_165+38delinsGA	ENSP00000425474.3:n.165+37_165+38delinsGA...
ENST00000510895.7:n.1026+37_1026+38delinsGA
ENST00000629193.3:c.789+37_789+38delinsGA	ENSP00000486535.2:n.789+37_789+38delinsGA...
ENST00000681968.1:c.396+37_396+38delinsGA	ENSP00000508143.1:n.396+37_396+38delinsGA...
ENST00000682045.1:c.759+37_759+38delinsGA	ENSP00000507329.1:n.759+37_759+38delinsGA...
ENST00000682214.1:c.510+37_510+38delinsGA	ENSP00000507336.1:n.510+37_510+38delinsGA...
ENST00000682499.1:n.1724+37_1724+38delinsGA
ENST00000682541.1:c.903+37_903+38delinsGA	ENSP00000507673.1:n.903+37_903+38delinsGA...
ENST00000682687.1:c.903+37_903+38delinsGA	ENSP00000507945.1:n.903+37_903+38delinsGA...
ENST00000682727.1:c.903+37_903+38delinsGA	ENSP00000507393.1:n.903+37_903+38delinsGA...
ENST00000682876.1:c.1032+37_1032+38delinsGA	ENSP00000508389.1:n.1032+37_1032+38delins...
ENST00000683098.1:c.803+2894_803+2895delinsGA	ENSP00000507670.1:n.803+2894_803+2895deli...
ENST00000683258.1:c.*624+37_*624+38delinsGA	ENSP00000507448.1:n.*624+37_*624+38delins...
ENST00000683339.1:c.687+37_687+38delinsGA	ENSP00000507758.1:n.687+37_687+38delinsGA...
ENST00000683403.1:c.814-72_814-71delinsGA	ENSP00000507896.1:n.814-72_814-71delinsGA...
ENST00000683429.1:c.510+37_510+38delinsGA	ENSP00000507697.1:n.510+37_510+38delinsGA...
ENST00000683665.1:c.903+37_903+38delinsGA	ENSP00000507068.1:n.903+37_903+38delinsGA...
ENST00000683789.1:c.789+37_789+38delinsGA	ENSP00000507012.1:n.789+37_789+38delinsGA...
ENST00000683847.1:n.747+37_747+38delinsGA
ENST00000683882.1:c.903+37_903+38delinsGA	ENSP00000506735.1:n.903+37_903+38delinsGA...
ENST00000684024.1:c.*574+37_*574+38delinsGA	ENSP00000507175.1:n.*574+37_*574+38delins...
ENST00000684254.1:c.*629+37_*629+38delinsGA	ENSP00000508001.1:n.*629+37_*629+38delins...
ENST00000684310.1:c.165+37_165+38delinsGA	ENSP00000507550.1:n.165+37_165+38delinsGA...
ENST00000684530.1:c.165+37_165+38delinsGA	ENSP00000507439.1:n.165+37_165+38delinsGA...
ENST00000684652.1:n.1905+37_1905+38delinsGA
ENST00000340941.11:c.903+37_903+38delinsGA MANE Select	ENSP00000343657.6:n.903+37_903+38delinsGA...
ENST00000340941.10:c.903+37_903+38delinsGA	ENSP00000343657.6:n.903+37_903+38delinsGA...
ENST00000505435.3:n.254+37_254+38delinsGA
ENST00000505787.7:n.754_755delinsGA
ENST00000509358.6:c.903+37_903+38delinsGA	ENSP00000420994.2:n.903+37_903+38delinsGA...
ENST00000509539.2:c.228+37_228+38delinsGA	ENSP00000425474.2:n.228+37_228+38delinsGA...
ENST00000510895.6:n.517+37_517+38delinsGA
ENST00000512218.6:c.789+37_789+38delinsGA	ENSP00000423202.2:n.789+37_789+38delinsGA...
ENST00000629193.2:c.789+37_789+38delinsGA	ENSP00000486535.1:n.789+37_789+38delinsGA...
NM_022132.4:c.903+37_903+38delinsGA	NP_071415.1:n.903+37_903+38delinsGA
XM_005248567.1:c.789+37_789+38delinsGA	XP_005248624.1:n.789+37_789+38delinsGA
XM_011543528.1:c.903+37_903+38delinsGA	XP_011541830.1:n.903+37_903+38delinsGA
XM_011543529.1:c.903+37_903+38delinsGA	XP_011541831.1:n.903+37_903+38delinsGA
NM_001363147.1:c.789+37_789+38delinsGA	NP_001350076.1:n.789+37_789+38delinsGA
XM_011543529.2:c.903+37_903+38delinsGA	XP_011541831.1:n.903+37_903+38delinsGA
XM_017009688.1:c.903+37_903+38delinsGA	XP_016865177.1:n.903+37_903+38delinsGA
XR_001742172.1:n.943+37_943+38delinsGA
NM_022132.5:c.903+37_903+38delinsGA MANE Select	NP_071415.1:n.903+37_903+38delinsGA