Canonical Allele Identifier: CA1425382223

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037281C= , CM000665.2:g.183037281C=	GRCh38
NC_000003.11:g.182755069C= , CM000665.1:g.182755069C=	GRCh37
NC_000003.10:g.184237763C=	NCBI36
NG_008100.1:g.67297G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1531G= MANE Select	ENSP00000265594.4:p.Ala511=
ENST00000265594.8:c.1531G=	ENSP00000265594.4:p.Ala511=
ENST00000476176.5:c.1390G=	ENSP00000420433.1:p.Ala464=
ENST00000489909.1:n.75G=
ENST00000492597.5:c.1204G=	ENSP00000419898.1:p.Ala402=
ENST00000495767.5:c.*1112G=	ENSP00000419658.1:n.*1112G=
ENST00000497830.5:c.*1128G=	ENSP00000420088.1:n.*1128G=
ENST00000497959.5:c.1263+1745G=	ENSP00000420648.1:n.1263+1745G=
ENST00000539926.5:c.1081G=	ENSP00000441253.2:p.Ala361=
ENST00000610757.4:c.1081G=	ENSP00000480435.1:p.Ala361=
ENST00000629669.2:c.1263+1745G=	ENSP00000486824.1:n.1263+1745G=
NM_001293273.1:c.1180G=	NP_001280202.1:p.Ala394=
NM_020166.4:c.1531G=	NP_064551.3:p.Ala511=
NR_120639.1:n.1445G=
NR_120640.1:n.2044+1745G=
XM_006713702.1:c.1204G=	XP_006713765.1:p.Ala402=
XM_011512992.1:c.1417G=	XP_011511294.1:p.Ala473=
XM_011512993.1:c.1377+1745G=	XP_011511295.1:n.1377+1745G=
XR_241502.2:n.1524+1745G=
XR_924159.1:n.1678G=
NM_001363880.1:c.1204G=	NP_001350809.1:p.Ala402=
XM_011512992.2:c.1417G=	XP_011511294.1:p.Ala473=
XR_001740207.2:n.1654G=
XR_001740208.2:n.1654G=
XR_001740209.2:n.1470+1745G=
XR_001740210.1:n.1484G=
XR_002959553.1:n.1654G=
XR_002959554.1:n.1500+1745G=
XR_241502.3:n.1470+1745G=
NM_020166.5:c.1531G= MANE Select	NP_064551.3:p.Ala511=
NM_001293273.2:c.1180G=	NP_001280202.1:p.Ala394=
NR_120639.2:n.1354G=
NR_120640.2:n.2044+1745G=