Canonical Allele Identifier: CA1425382280

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037396G= , CM000665.2:g.183037396G=	GRCh38
NC_000003.11:g.182755184G= , CM000665.1:g.182755184G=	GRCh37
NC_000003.10:g.184237878G=	NCBI36
NG_008100.1:g.67182C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1416C= MANE Select	ENSP00000265594.4:p.Asn472=
ENST00000265594.8:c.1416C=	ENSP00000265594.4:p.Asn472=
ENST00000476176.5:c.1275C=	ENSP00000420433.1:p.Asn425=
ENST00000492597.5:c.1089C=	ENSP00000419898.1:p.Asn363=
ENST00000495767.5:c.*997C=	ENSP00000419658.1:n.*997C=
ENST00000497830.5:c.*1013C=	ENSP00000420088.1:n.*1013C=
ENST00000497959.5:c.1263+1630C=	ENSP00000420648.1:n.1263+1630C=
ENST00000539926.5:c.966C=	ENSP00000441253.2:p.Asn322=
ENST00000610757.4:c.966C=	ENSP00000480435.1:p.Asn322=
ENST00000629669.2:c.1263+1630C=	ENSP00000486824.1:n.1263+1630C=
NM_001293273.1:c.1065C=	NP_001280202.1:p.Asn355=
NM_020166.4:c.1416C=	NP_064551.3:p.Asn472=
NR_120639.1:n.1330C=
NR_120640.1:n.2044+1630C=
XM_006713702.1:c.1089C=	XP_006713765.1:p.Asn363=
XM_011512992.1:c.1302C=	XP_011511294.1:p.Asn434=
XM_011512993.1:c.1377+1630C=	XP_011511295.1:n.1377+1630C=
XR_241502.2:n.1524+1630C=
XR_924159.1:n.1563C=
NM_001363880.1:c.1089C=	NP_001350809.1:p.Asn363=
XM_011512992.2:c.1302C=	XP_011511294.1:p.Asn434=
XR_001740207.2:n.1539C=
XR_001740208.2:n.1539C=
XR_001740209.2:n.1470+1630C=
XR_001740210.1:n.1369C=
XR_002959553.1:n.1539C=
XR_002959554.1:n.1500+1630C=
XR_241502.3:n.1470+1630C=
NM_020166.5:c.1416C= MANE Select	NP_064551.3:p.Asn472=
NM_001293273.2:c.1065C=	NP_001280202.1:p.Asn355=
NR_120639.2:n.1239C=
NR_120640.2:n.2044+1630C=