Canonical Allele Identifier: CA1425382980

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039118G= , CM000665.2:g.183039118G=	GRCh38
NC_000003.11:g.182756906G= , CM000665.1:g.182756906G=	GRCh37
NC_000003.10:g.184239600G=	NCBI36
NG_008100.1:g.65460C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1285C= MANE Select	ENSP00000265594.4:p.His429=
ENST00000265594.8:c.1285C=	ENSP00000265594.4:p.His429=
ENST00000476176.5:c.1144C=	ENSP00000420433.1:p.His382=
ENST00000492597.5:c.958C=	ENSP00000419898.1:p.His320=
ENST00000495767.5:c.*866C=	ENSP00000419658.1:n.*866C=
ENST00000497830.5:c.*882C=	ENSP00000420088.1:n.*882C=
ENST00000497959.5:c.1171C=	ENSP00000420648.1:p.His391=
ENST00000539926.5:c.835C=	ENSP00000441253.2:p.His279=
ENST00000610757.4:c.835C=	ENSP00000480435.1:p.His279=
ENST00000629669.2:c.1171C=	ENSP00000486824.1:p.His391=
NM_001293273.1:c.934C=	NP_001280202.1:p.His312=
NM_020166.4:c.1285C=	NP_064551.3:p.His429=
NR_120639.1:n.1199C=
NR_120640.1:n.1952C=
XM_006713702.1:c.958C=	XP_006713765.1:p.His320=
XM_011512992.1:c.1171C=	XP_011511294.1:p.His391=
XM_011512993.1:c.1285C=	XP_011511295.1:p.His429=
XR_241502.2:n.1432C=
XR_924159.1:n.1432C=
NM_001363880.1:c.958C=	NP_001350809.1:p.His320=
XM_011512992.2:c.1171C=	XP_011511294.1:p.His391=
XR_001740207.2:n.1408C=
XR_001740208.2:n.1408C=
XR_001740209.2:n.1378C=
XR_001740210.1:n.1238C=
XR_002959553.1:n.1408C=
XR_002959554.1:n.1408C=
XR_241502.3:n.1378C=
NM_020166.5:c.1285C= MANE Select	NP_064551.3:p.His429=
NM_001293273.2:c.934C=	NP_001280202.1:p.His312=
NR_120639.2:n.1108C=
NR_120640.2:n.1952C=