Canonical Allele Identifier: CA1425382984

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039126A= , CM000665.2:g.183039126A=	GRCh38
NC_000003.11:g.182756914A= , CM000665.1:g.182756914A=	GRCh37
NC_000003.10:g.184239608A=	NCBI36
NG_008100.1:g.65452T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1277T= MANE Select	ENSP00000265594.4:p.Val426=
ENST00000265594.8:c.1277T=	ENSP00000265594.4:p.Val426=
ENST00000476176.5:c.1136T=	ENSP00000420433.1:p.Val379=
ENST00000492597.5:c.950T=	ENSP00000419898.1:p.Val317=
ENST00000495767.5:c.*858T=	ENSP00000419658.1:n.*858T=
ENST00000497830.5:c.*874T=	ENSP00000420088.1:n.*874T=
ENST00000497959.5:c.1163T=	ENSP00000420648.1:p.Val388=
ENST00000539926.5:c.827T=	ENSP00000441253.2:p.Val276=
ENST00000610757.4:c.827T=	ENSP00000480435.1:p.Val276=
ENST00000629669.2:c.1163T=	ENSP00000486824.1:p.Val388=
NM_001293273.1:c.926T=	NP_001280202.1:p.Val309=
NM_020166.4:c.1277T=	NP_064551.3:p.Val426=
NR_120639.1:n.1191T=
NR_120640.1:n.1944T=
XM_006713702.1:c.950T=	XP_006713765.1:p.Val317=
XM_011512992.1:c.1163T=	XP_011511294.1:p.Val388=
XM_011512993.1:c.1277T=	XP_011511295.1:p.Val426=
XR_241502.2:n.1424T=
XR_924159.1:n.1424T=
NM_001363880.1:c.950T=	NP_001350809.1:p.Val317=
XM_011512992.2:c.1163T=	XP_011511294.1:p.Val388=
XR_001740207.2:n.1400T=
XR_001740208.2:n.1400T=
XR_001740209.2:n.1370T=
XR_001740210.1:n.1230T=
XR_002959553.1:n.1400T=
XR_002959554.1:n.1400T=
XR_241502.3:n.1370T=
NM_020166.5:c.1277T= MANE Select	NP_064551.3:p.Val426=
NM_001293273.2:c.926T=	NP_001280202.1:p.Val309=
NR_120639.2:n.1100T=
NR_120640.2:n.1944T=