Canonical Allele Identifier: CA1425382972

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039093A= , CM000665.2:g.183039093A=	GRCh38
NC_000003.11:g.182756881A= , CM000665.1:g.182756881A=	GRCh37
NC_000003.10:g.184239575A=	NCBI36
NG_008100.1:g.65485T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1310T= MANE Select	ENSP00000265594.4:p.Leu437=
ENST00000265594.8:c.1310T=	ENSP00000265594.4:p.Leu437=
ENST00000476176.5:c.1169T=	ENSP00000420433.1:p.Leu390=
ENST00000492597.5:c.983T=	ENSP00000419898.1:p.Leu328=
ENST00000495767.5:c.*891T=	ENSP00000419658.1:n.*891T=
ENST00000497830.5:c.*907T=	ENSP00000420088.1:n.*907T=
ENST00000497959.5:c.1196T=	ENSP00000420648.1:p.Leu399=
ENST00000539926.5:c.860T=	ENSP00000441253.2:p.Leu287=
ENST00000610757.4:c.860T=	ENSP00000480435.1:p.Leu287=
ENST00000629669.2:c.1196T=	ENSP00000486824.1:p.Leu399=
NM_001293273.1:c.959T=	NP_001280202.1:p.Leu320=
NM_020166.4:c.1310T=	NP_064551.3:p.Leu437=
NR_120639.1:n.1224T=
NR_120640.1:n.1977T=
XM_006713702.1:c.983T=	XP_006713765.1:p.Leu328=
XM_011512992.1:c.1196T=	XP_011511294.1:p.Leu399=
XM_011512993.1:c.1310T=	XP_011511295.1:p.Leu437=
XR_241502.2:n.1457T=
XR_924159.1:n.1457T=
NM_001363880.1:c.983T=	NP_001350809.1:p.Leu328=
XM_011512992.2:c.1196T=	XP_011511294.1:p.Leu399=
XR_001740207.2:n.1433T=
XR_001740208.2:n.1433T=
XR_001740209.2:n.1403T=
XR_001740210.1:n.1263T=
XR_002959553.1:n.1433T=
XR_002959554.1:n.1433T=
XR_241502.3:n.1403T=
NM_020166.5:c.1310T= MANE Select	NP_064551.3:p.Leu437=
NM_001293273.2:c.959T=	NP_001280202.1:p.Leu320=
NR_120639.2:n.1133T=
NR_120640.2:n.1977T=