Canonical Allele Identifier: CA1425382964

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039072C= , CM000665.2:g.183039072C=	GRCh38
NC_000003.11:g.182756860C= , CM000665.1:g.182756860C=	GRCh37
NC_000003.10:g.184239554C=	NCBI36
NG_008100.1:g.65506G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1331G= MANE Select	ENSP00000265594.4:p.Arg444=
ENST00000265594.8:c.1331G=	ENSP00000265594.4:p.Arg444=
ENST00000476176.5:c.1190G=	ENSP00000420433.1:p.Arg397=
ENST00000492597.5:c.1004G=	ENSP00000419898.1:p.Arg335=
ENST00000495767.5:c.*912G=	ENSP00000419658.1:n.*912G=
ENST00000497830.5:c.*928G=	ENSP00000420088.1:n.*928G=
ENST00000497959.5:c.1217G=	ENSP00000420648.1:p.Arg406=
ENST00000539926.5:c.881G=	ENSP00000441253.2:p.Arg294=
ENST00000610757.4:c.881G=	ENSP00000480435.1:p.Arg294=
ENST00000629669.2:c.1217G=	ENSP00000486824.1:p.Arg406=
NM_001293273.1:c.980G=	NP_001280202.1:p.Arg327=
NM_020166.4:c.1331G=	NP_064551.3:p.Arg444=
NR_120639.1:n.1245G=
NR_120640.1:n.1998G=
XM_006713702.1:c.1004G=	XP_006713765.1:p.Arg335=
XM_011512992.1:c.1217G=	XP_011511294.1:p.Arg406=
XM_011512993.1:c.1331G=	XP_011511295.1:p.Arg444=
XR_241502.2:n.1478G=
XR_924159.1:n.1478G=
NM_001363880.1:c.1004G=	NP_001350809.1:p.Arg335=
XM_011512992.2:c.1217G=	XP_011511294.1:p.Arg406=
XR_001740207.2:n.1454G=
XR_001740208.2:n.1454G=
XR_001740209.2:n.1424G=
XR_001740210.1:n.1284G=
XR_002959553.1:n.1454G=
XR_002959554.1:n.1454G=
XR_241502.3:n.1424G=
NM_020166.5:c.1331G= MANE Select	NP_064551.3:p.Arg444=
NM_001293273.2:c.980G=	NP_001280202.1:p.Arg327=
NR_120639.2:n.1154G=
NR_120640.2:n.1998G=