Canonical Allele Identifier: CA1425382955

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039058T= , CM000665.2:g.183039058T=	GRCh38
NC_000003.11:g.182756846T= , CM000665.1:g.182756846T=	GRCh37
NC_000003.10:g.184239540T=	NCBI36
NG_008100.1:g.65520A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1345A= MANE Select	ENSP00000265594.4:p.Thr449=
ENST00000265594.8:c.1345A=	ENSP00000265594.4:p.Thr449=
ENST00000476176.5:c.1204A=	ENSP00000420433.1:p.Thr402=
ENST00000492597.5:c.1018A=	ENSP00000419898.1:p.Thr340=
ENST00000495767.5:c.*926A=	ENSP00000419658.1:n.*926A=
ENST00000497830.5:c.*942A=	ENSP00000420088.1:n.*942A=
ENST00000497959.5:c.1231A=	ENSP00000420648.1:p.Thr411=
ENST00000539926.5:c.895A=	ENSP00000441253.2:p.Thr299=
ENST00000610757.4:c.895A=	ENSP00000480435.1:p.Thr299=
ENST00000629669.2:c.1231A=	ENSP00000486824.1:p.Thr411=
NM_001293273.1:c.994A=	NP_001280202.1:p.Thr332=
NM_020166.4:c.1345A=	NP_064551.3:p.Thr449=
NR_120639.1:n.1259A=
NR_120640.1:n.2012A=
XM_006713702.1:c.1018A=	XP_006713765.1:p.Thr340=
XM_011512992.1:c.1231A=	XP_011511294.1:p.Thr411=
XM_011512993.1:c.1345A=	XP_011511295.1:p.Thr449=
XR_241502.2:n.1492A=
XR_924159.1:n.1492A=
NM_001363880.1:c.1018A=	NP_001350809.1:p.Thr340=
XM_011512992.2:c.1231A=	XP_011511294.1:p.Thr411=
XR_001740207.2:n.1468A=
XR_001740208.2:n.1468A=
XR_001740209.2:n.1438A=
XR_001740210.1:n.1298A=
XR_002959553.1:n.1468A=
XR_002959554.1:n.1468A=
XR_241502.3:n.1438A=
NM_020166.5:c.1345A= MANE Select	NP_064551.3:p.Thr449=
NM_001293273.2:c.994A=	NP_001280202.1:p.Thr332=
NR_120639.2:n.1168A=
NR_120640.2:n.2012A=