Canonical Allele Identifier: CA1425382974

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039098C= , CM000665.2:g.183039098C=	GRCh38
NC_000003.11:g.182756886C= , CM000665.1:g.182756886C=	GRCh37
NC_000003.10:g.184239580C=	NCBI36
NG_008100.1:g.65480G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1305G= MANE Select	ENSP00000265594.4:p.Ala435=
ENST00000265594.8:c.1305G=	ENSP00000265594.4:p.Ala435=
ENST00000476176.5:c.1164G=	ENSP00000420433.1:p.Ala388=
ENST00000492597.5:c.978G=	ENSP00000419898.1:p.Ala326=
ENST00000495767.5:c.*886G=	ENSP00000419658.1:n.*886G=
ENST00000497830.5:c.*902G=	ENSP00000420088.1:n.*902G=
ENST00000497959.5:c.1191G=	ENSP00000420648.1:p.Ala397=
ENST00000539926.5:c.855G=	ENSP00000441253.2:p.Ala285=
ENST00000610757.4:c.855G=	ENSP00000480435.1:p.Ala285=
ENST00000629669.2:c.1191G=	ENSP00000486824.1:p.Ala397=
NM_001293273.1:c.954G=	NP_001280202.1:p.Ala318=
NM_020166.4:c.1305G=	NP_064551.3:p.Ala435=
NR_120639.1:n.1219G=
NR_120640.1:n.1972G=
XM_006713702.1:c.978G=	XP_006713765.1:p.Ala326=
XM_011512992.1:c.1191G=	XP_011511294.1:p.Ala397=
XM_011512993.1:c.1305G=	XP_011511295.1:p.Ala435=
XR_241502.2:n.1452G=
XR_924159.1:n.1452G=
NM_001363880.1:c.978G=	NP_001350809.1:p.Ala326=
XM_011512992.2:c.1191G=	XP_011511294.1:p.Ala397=
XR_001740207.2:n.1428G=
XR_001740208.2:n.1428G=
XR_001740209.2:n.1398G=
XR_001740210.1:n.1258G=
XR_002959553.1:n.1428G=
XR_002959554.1:n.1428G=
XR_241502.3:n.1398G=
NM_020166.5:c.1305G= MANE Select	NP_064551.3:p.Ala435=
NM_001293273.2:c.954G=	NP_001280202.1:p.Ala318=
NR_120639.2:n.1128G=
NR_120640.2:n.1972G=