Canonical Allele Identifier: CA1425382966

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039076C= , CM000665.2:g.183039076C=	GRCh38
NC_000003.11:g.182756864C= , CM000665.1:g.182756864C=	GRCh37
NC_000003.10:g.184239558C=	NCBI36
NG_008100.1:g.65502G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1327G= MANE Select	ENSP00000265594.4:p.Asp443=
ENST00000265594.8:c.1327G=	ENSP00000265594.4:p.Asp443=
ENST00000476176.5:c.1186G=	ENSP00000420433.1:p.Asp396=
ENST00000492597.5:c.1000G=	ENSP00000419898.1:p.Asp334=
ENST00000495767.5:c.*908G=	ENSP00000419658.1:n.*908G=
ENST00000497830.5:c.*924G=	ENSP00000420088.1:n.*924G=
ENST00000497959.5:c.1213G=	ENSP00000420648.1:p.Asp405=
ENST00000539926.5:c.877G=	ENSP00000441253.2:p.Asp293=
ENST00000610757.4:c.877G=	ENSP00000480435.1:p.Asp293=
ENST00000629669.2:c.1213G=	ENSP00000486824.1:p.Asp405=
NM_001293273.1:c.976G=	NP_001280202.1:p.Asp326=
NM_020166.4:c.1327G=	NP_064551.3:p.Asp443=
NR_120639.1:n.1241G=
NR_120640.1:n.1994G=
XM_006713702.1:c.1000G=	XP_006713765.1:p.Asp334=
XM_011512992.1:c.1213G=	XP_011511294.1:p.Asp405=
XM_011512993.1:c.1327G=	XP_011511295.1:p.Asp443=
XR_241502.2:n.1474G=
XR_924159.1:n.1474G=
NM_001363880.1:c.1000G=	NP_001350809.1:p.Asp334=
XM_011512992.2:c.1213G=	XP_011511294.1:p.Asp405=
XR_001740207.2:n.1450G=
XR_001740208.2:n.1450G=
XR_001740209.2:n.1420G=
XR_001740210.1:n.1280G=
XR_002959553.1:n.1450G=
XR_002959554.1:n.1450G=
XR_241502.3:n.1420G=
NM_020166.5:c.1327G= MANE Select	NP_064551.3:p.Asp443=
NM_001293273.2:c.976G=	NP_001280202.1:p.Asp326=
NR_120639.2:n.1150G=
NR_120640.2:n.1994G=