Canonical Allele Identifier: CA1425382971

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039089G= , CM000665.2:g.183039089G=	GRCh38
NC_000003.11:g.182756877G= , CM000665.1:g.182756877G=	GRCh37
NC_000003.10:g.184239571G=	NCBI36
NG_008100.1:g.65489C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1314C= MANE Select	ENSP00000265594.4:p.Val438=
ENST00000265594.8:c.1314C=	ENSP00000265594.4:p.Val438=
ENST00000476176.5:c.1173C=	ENSP00000420433.1:p.Val391=
ENST00000492597.5:c.987C=	ENSP00000419898.1:p.Val329=
ENST00000495767.5:c.*895C=	ENSP00000419658.1:n.*895C=
ENST00000497830.5:c.*911C=	ENSP00000420088.1:n.*911C=
ENST00000497959.5:c.1200C=	ENSP00000420648.1:p.Val400=
ENST00000539926.5:c.864C=	ENSP00000441253.2:p.Val288=
ENST00000610757.4:c.864C=	ENSP00000480435.1:p.Val288=
ENST00000629669.2:c.1200C=	ENSP00000486824.1:p.Val400=
NM_001293273.1:c.963C=	NP_001280202.1:p.Val321=
NM_020166.4:c.1314C=	NP_064551.3:p.Val438=
NR_120639.1:n.1228C=
NR_120640.1:n.1981C=
XM_006713702.1:c.987C=	XP_006713765.1:p.Val329=
XM_011512992.1:c.1200C=	XP_011511294.1:p.Val400=
XM_011512993.1:c.1314C=	XP_011511295.1:p.Val438=
XR_241502.2:n.1461C=
XR_924159.1:n.1461C=
NM_001363880.1:c.987C=	NP_001350809.1:p.Val329=
XM_011512992.2:c.1200C=	XP_011511294.1:p.Val400=
XR_001740207.2:n.1437C=
XR_001740208.2:n.1437C=
XR_001740209.2:n.1407C=
XR_001740210.1:n.1267C=
XR_002959553.1:n.1437C=
XR_002959554.1:n.1437C=
XR_241502.3:n.1407C=
NM_020166.5:c.1314C= MANE Select	NP_064551.3:p.Val438=
NM_001293273.2:c.963C=	NP_001280202.1:p.Val321=
NR_120639.2:n.1137C=
NR_120640.2:n.1981C=