Canonical Allele Identifier: CA1425384069

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183041679T= , CM000665.2:g.183041679T=	GRCh38
NC_000003.11:g.182759467T= , CM000665.1:g.182759467T=	GRCh37
NC_000003.10:g.184242161T=	NCBI36
NG_008100.1:g.62899A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1155A= MANE Select	ENSP00000265594.4:p.Arg385=
ENST00000265594.8:c.1155A=	ENSP00000265594.4:p.Arg385=
ENST00000476176.5:c.1014A=	ENSP00000420433.1:p.Arg338=
ENST00000492597.5:c.828A=	ENSP00000419898.1:p.Arg276=
ENST00000495767.5:c.*736A=	ENSP00000419658.1:n.*736A=
ENST00000497830.5:c.*752A=	ENSP00000420088.1:n.*752A=
ENST00000497959.5:c.1041A=	ENSP00000420648.1:p.Arg347=
ENST00000539926.5:c.705A=	ENSP00000441253.2:p.Arg235=
ENST00000610757.4:c.705A=	ENSP00000480435.1:p.Arg235=
ENST00000629669.2:c.1041A=	ENSP00000486824.1:p.Arg347=
NM_001293273.1:c.804A=	NP_001280202.1:p.Arg268=
NM_020166.4:c.1155A=	NP_064551.3:p.Arg385=
NR_120639.1:n.1069A=
NR_120640.1:n.1822A=
XM_006713702.1:c.828A=	XP_006713765.1:p.Arg276=
XM_011512992.1:c.1041A=	XP_011511294.1:p.Arg347=
XM_011512993.1:c.1155A=	XP_011511295.1:p.Arg385=
XR_241502.2:n.1302A=
XR_924159.1:n.1302A=
NM_001363880.1:c.828A=	NP_001350809.1:p.Arg276=
XM_011512992.2:c.1041A=	XP_011511294.1:p.Arg347=
XR_001740207.2:n.1278A=
XR_001740208.2:n.1278A=
XR_001740209.2:n.1248A=
XR_001740210.1:n.1108A=
XR_002959553.1:n.1278A=
XR_002959554.1:n.1278A=
XR_241502.3:n.1248A=
NM_020166.5:c.1155A= MANE Select	NP_064551.3:p.Arg385=
NM_001293273.2:c.804A=	NP_001280202.1:p.Arg268=
NR_120639.2:n.978A=
NR_120640.2:n.1822A=