Canonical Allele Identifier: CA1425382328

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037525_183037526delinsCT , CM000665.2:g.183037525_183037526delinsCT	GRCh38
NC_000003.11:g.182755313_182755314delinsCT , CM000665.1:g.182755313_182755314delinsCT	GRCh37
NC_000003.10:g.184238007_184238008delinsCT	NCBI36
NG_008100.1:g.67052_67053delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1378-92_1378-91delinsAG MANE Select	ENSP00000265594.4:n.1378-92_1378-91delinsAG
ENST00000265594.8:c.1378-92_1378-91delinsAG	ENSP00000265594.4:n.1378-92_1378-91delinsAG
ENST00000476176.5:c.1237-92_1237-91delinsAG	ENSP00000420433.1:n.1237-92_1237-91delinsAG
ENST00000492597.5:c.1051-92_1051-91delinsAG	ENSP00000419898.1:n.1051-92_1051-91delinsAG
ENST00000495767.5:c.*959-92_*959-91delinsAG	ENSP00000419658.1:n.*959-92_*959-91delinsAG
ENST00000497830.5:c.*975-92_*975-91delinsAG	ENSP00000420088.1:n.*975-92_*975-91delinsAG
ENST00000497959.5:c.1263+1500_1263+1501delinsAG	ENSP00000420648.1:n.1263+1500_1263+1501delinsAG
ENST00000539926.5:c.928-92_928-91delinsAG	ENSP00000441253.2:n.928-92_928-91delinsAG
ENST00000610757.4:c.928-92_928-91delinsAG	ENSP00000480435.1:n.928-92_928-91delinsAG
ENST00000629669.2:c.1263+1500_1263+1501delinsAG	ENSP00000486824.1:n.1263+1500_1263+1501delinsAG
NM_001293273.1:c.1027-92_1027-91delinsAG	NP_001280202.1:n.1027-92_1027-91delinsAG
NM_020166.4:c.1378-92_1378-91delinsAG	NP_064551.3:n.1378-92_1378-91delinsAG
NR_120639.1:n.1292-92_1292-91delinsAG
NR_120640.1:n.2044+1500_2044+1501delinsAG
XM_006713702.1:c.1051-92_1051-91delinsAG	XP_006713765.1:n.1051-92_1051-91delinsAG
XM_011512992.1:c.1264-92_1264-91delinsAG	XP_011511294.1:n.1264-92_1264-91delinsAG
XM_011512993.1:c.1377+1500_1377+1501delinsAG	XP_011511295.1:n.1377+1500_1377+1501delinsAG
XR_241502.2:n.1524+1500_1524+1501delinsAG
XR_924159.1:n.1525-92_1525-91delinsAG
NM_001363880.1:c.1051-92_1051-91delinsAG	NP_001350809.1:n.1051-92_1051-91delinsAG
XM_011512992.2:c.1264-92_1264-91delinsAG	XP_011511294.1:n.1264-92_1264-91delinsAG
XR_001740207.2:n.1501-92_1501-91delinsAG
XR_001740208.2:n.1501-92_1501-91delinsAG
XR_001740209.2:n.1470+1500_1470+1501delinsAG
XR_001740210.1:n.1331-92_1331-91delinsAG
XR_002959553.1:n.1501-92_1501-91delinsAG
XR_002959554.1:n.1500+1500_1500+1501delinsAG
XR_241502.3:n.1470+1500_1470+1501delinsAG
NM_020166.5:c.1378-92_1378-91delinsAG MANE Select	NP_064551.3:n.1378-92_1378-91delinsAG
NM_001293273.2:c.1027-92_1027-91delinsAG	NP_001280202.1:n.1027-92_1027-91delinsAG
NR_120639.2:n.1201-92_1201-91delinsAG
NR_120640.2:n.2044+1500_2044+1501delinsAG