Canonical Allele Identifier: CA1425382308

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037450_183037451delinsAC , CM000665.2:g.183037450_183037451delinsAC	GRCh38
NC_000003.11:g.182755238_182755239delinsAC , CM000665.1:g.182755238_182755239delinsAC	GRCh37
NC_000003.10:g.184237932_184237933delinsAC	NCBI36
NG_008100.1:g.67127_67128delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1378-17_1378-16delinsGT MANE Select	ENSP00000265594.4:n.1378-17_1378-16delinsGT
ENST00000265594.8:c.1378-17_1378-16delinsGT	ENSP00000265594.4:n.1378-17_1378-16delinsGT
ENST00000476176.5:c.1237-17_1237-16delinsGT	ENSP00000420433.1:n.1237-17_1237-16delinsGT
ENST00000492597.5:c.1051-17_1051-16delinsGT	ENSP00000419898.1:n.1051-17_1051-16delinsGT
ENST00000495767.5:c.*959-17_*959-16delinsGT	ENSP00000419658.1:n.*959-17_*959-16delinsGT
ENST00000497830.5:c.*975-17_*975-16delinsGT	ENSP00000420088.1:n.*975-17_*975-16delinsGT
ENST00000497959.5:c.1263+1575_1263+1576delinsGT	ENSP00000420648.1:n.1263+1575_1263+1576delinsGT
ENST00000539926.5:c.928-17_928-16delinsGT	ENSP00000441253.2:n.928-17_928-16delinsGT
ENST00000610757.4:c.928-17_928-16delinsGT	ENSP00000480435.1:n.928-17_928-16delinsGT
ENST00000629669.2:c.1263+1575_1263+1576delinsGT	ENSP00000486824.1:n.1263+1575_1263+1576delinsGT
NM_001293273.1:c.1027-17_1027-16delinsGT	NP_001280202.1:n.1027-17_1027-16delinsGT
NM_020166.4:c.1378-17_1378-16delinsGT	NP_064551.3:n.1378-17_1378-16delinsGT
NR_120639.1:n.1292-17_1292-16delinsGT
NR_120640.1:n.2044+1575_2044+1576delinsGT
XM_006713702.1:c.1051-17_1051-16delinsGT	XP_006713765.1:n.1051-17_1051-16delinsGT
XM_011512992.1:c.1264-17_1264-16delinsGT	XP_011511294.1:n.1264-17_1264-16delinsGT
XM_011512993.1:c.1377+1575_1377+1576delinsGT	XP_011511295.1:n.1377+1575_1377+1576delinsGT
XR_241502.2:n.1524+1575_1524+1576delinsGT
XR_924159.1:n.1525-17_1525-16delinsGT
NM_001363880.1:c.1051-17_1051-16delinsGT	NP_001350809.1:n.1051-17_1051-16delinsGT
XM_011512992.2:c.1264-17_1264-16delinsGT	XP_011511294.1:n.1264-17_1264-16delinsGT
XR_001740207.2:n.1501-17_1501-16delinsGT
XR_001740208.2:n.1501-17_1501-16delinsGT
XR_001740209.2:n.1470+1575_1470+1576delinsGT
XR_001740210.1:n.1331-17_1331-16delinsGT
XR_002959553.1:n.1501-17_1501-16delinsGT
XR_002959554.1:n.1500+1575_1500+1576delinsGT
XR_241502.3:n.1470+1575_1470+1576delinsGT
NM_020166.5:c.1378-17_1378-16delinsGT MANE Select	NP_064551.3:n.1378-17_1378-16delinsGT
NM_001293273.2:c.1027-17_1027-16delinsGT	NP_001280202.1:n.1027-17_1027-16delinsGT
NR_120639.2:n.1201-17_1201-16delinsGT
NR_120640.2:n.2044+1575_2044+1576delinsGT