Canonical Allele Identifier: CA1554387654

Gene: MCCC2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.71634844_71634845delinsGT , CM000667.2:g.71634844_71634845delinsGT	GRCh38
NC_000005.9:g.70930671_70930672delinsGT , CM000667.1:g.70930671_70930672delinsGT	GRCh37
NC_000005.8:g.70966427_70966428delinsGT	NCBI36
NG_008882.1:g.52557_52558delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000505435.4:n.760-99_760-98delinsGT
ENST00000505787.8:n.2644-99_2644-98delinsGT
ENST00000509358.7:c.804-99_804-98delinsGT	ENSP00000420994.3:n.804-99_804-98delinsGT
ENST00000509539.3:c.66-99_66-98delinsGT	ENSP00000425474.3:n.66-99_66-98delinsGT
ENST00000510895.7:n.927-99_927-98delinsGT
ENST00000629193.3:c.690-99_690-98delinsGT	ENSP00000486535.2:n.690-99_690-98delinsGT
ENST00000681968.1:c.297-99_297-98delinsGT	ENSP00000508143.1:n.297-99_297-98delinsGT
ENST00000682045.1:c.660-99_660-98delinsGT	ENSP00000507329.1:n.660-99_660-98delinsGT
ENST00000682214.1:c.411-99_411-98delinsGT	ENSP00000507336.1:n.411-99_411-98delinsGT
ENST00000682499.1:n.1625-99_1625-98delinsGT
ENST00000682541.1:c.804-99_804-98delinsGT	ENSP00000507673.1:n.804-99_804-98delinsGT
ENST00000682687.1:c.804-99_804-98delinsGT	ENSP00000507945.1:n.804-99_804-98delinsGT
ENST00000682727.1:c.804-99_804-98delinsGT	ENSP00000507393.1:n.804-99_804-98delinsGT
ENST00000682876.1:c.933-99_933-98delinsGT	ENSP00000508389.1:n.933-99_933-98delinsGT
ENST00000683098.1:c.803+2659_803+2660delinsGT	ENSP00000507670.1:n.803+2659_803+2660delinsGT
ENST00000683258.1:c.*525-99_*525-98delinsGT	ENSP00000507448.1:n.*525-99_*525-98delinsGT
ENST00000683339.1:c.588-99_588-98delinsGT	ENSP00000507758.1:n.588-99_588-98delinsGT
ENST00000683403.1:c.804-99_804-98delinsGT	ENSP00000507896.1:n.804-99_804-98delinsGT
ENST00000683429.1:c.411-99_411-98delinsGT	ENSP00000507697.1:n.411-99_411-98delinsGT
ENST00000683665.1:c.804-99_804-98delinsGT	ENSP00000507068.1:n.804-99_804-98delinsGT
ENST00000683789.1:c.690-99_690-98delinsGT	ENSP00000507012.1:n.690-99_690-98delinsGT
ENST00000683847.1:n.648-99_648-98delinsGT
ENST00000683882.1:c.804-99_804-98delinsGT	ENSP00000506735.1:n.804-99_804-98delinsGT
ENST00000684024.1:c.*475-99_*475-98delinsGT	ENSP00000507175.1:n.*475-99_*475-98delinsGT
ENST00000684254.1:c.*530-99_*530-98delinsGT	ENSP00000508001.1:n.*530-99_*530-98delinsGT
ENST00000684310.1:c.66-99_66-98delinsGT	ENSP00000507550.1:n.66-99_66-98delinsGT
ENST00000684530.1:c.66-99_66-98delinsGT	ENSP00000507439.1:n.66-99_66-98delinsGT
ENST00000684652.1:n.1707_1708delinsGT
ENST00000340941.11:c.804-99_804-98delinsGT MANE Select	ENSP00000343657.6:n.804-99_804-98delinsGT
ENST00000340941.10:c.804-99_804-98delinsGT	ENSP00000343657.6:n.804-99_804-98delinsGT
ENST00000505435.3:n.155-99_155-98delinsGT
ENST00000505787.7:n.618-99_618-98delinsGT
ENST00000509358.6:c.804-99_804-98delinsGT	ENSP00000420994.2:n.804-99_804-98delinsGT
ENST00000509539.2:c.129-99_129-98delinsGT	ENSP00000425474.2:n.129-99_129-98delinsGT
ENST00000510895.6:n.418-99_418-98delinsGT
ENST00000512218.6:c.690-99_690-98delinsGT	ENSP00000423202.2:n.690-99_690-98delinsGT
ENST00000629193.2:c.690-99_690-98delinsGT	ENSP00000486535.1:n.690-99_690-98delinsGT
NM_022132.4:c.804-99_804-98delinsGT	NP_071415.1:n.804-99_804-98delinsGT
XM_005248567.1:c.690-99_690-98delinsGT	XP_005248624.1:n.690-99_690-98delinsGT
XM_011543528.1:c.804-99_804-98delinsGT	XP_011541830.1:n.804-99_804-98delinsGT
XM_011543529.1:c.804-99_804-98delinsGT	XP_011541831.1:n.804-99_804-98delinsGT
NM_001363147.1:c.690-99_690-98delinsGT	NP_001350076.1:n.690-99_690-98delinsGT
XM_011543529.2:c.804-99_804-98delinsGT	XP_011541831.1:n.804-99_804-98delinsGT
XM_017009688.1:c.804-99_804-98delinsGT	XP_016865177.1:n.804-99_804-98delinsGT
XR_001742172.1:n.844-99_844-98delinsGT
NM_022132.5:c.804-99_804-98delinsGT MANE Select	NP_071415.1:n.804-99_804-98delinsGT