Canonical Allele Identifier: CA1425383121

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039441A= , CM000665.2:g.183039441A=	GRCh38
NC_000003.11:g.182757229A= , CM000665.1:g.182757229A=	GRCh37
NC_000003.10:g.184239923A=	NCBI36
NG_008100.1:g.65137T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1268-306T= MANE Select	ENSP00000265594.4:n.1268-306T=
ENST00000265594.8:c.1268-306T=	ENSP00000265594.4:n.1268-306T=
ENST00000476176.5:c.1127-306T=	ENSP00000420433.1:n.1127-306T=
ENST00000492597.5:c.941-306T=	ENSP00000419898.1:n.941-306T=
ENST00000495767.5:c.*849-306T=	ENSP00000419658.1:n.*849-306T=
ENST00000497830.5:c.*865-306T=	ENSP00000420088.1:n.*865-306T=
ENST00000497959.5:c.1154-306T=	ENSP00000420648.1:n.1154-306T=
ENST00000539926.5:c.818-306T=	ENSP00000441253.2:n.818-306T=
ENST00000610757.4:c.818-306T=	ENSP00000480435.1:n.818-306T=
ENST00000629669.2:c.1154-306T=	ENSP00000486824.1:n.1154-306T=
NM_001293273.1:c.917-306T=	NP_001280202.1:n.917-306T=
NM_020166.4:c.1268-306T=	NP_064551.3:n.1268-306T=
NR_120639.1:n.1182-306T=
NR_120640.1:n.1935-306T=
XM_006713702.1:c.941-306T=	XP_006713765.1:n.941-306T=
XM_011512992.1:c.1154-306T=	XP_011511294.1:n.1154-306T=
XM_011512993.1:c.1268-306T=	XP_011511295.1:n.1268-306T=
XR_241502.2:n.1415-306T=
XR_924159.1:n.1415-306T=
NM_001363880.1:c.941-306T=	NP_001350809.1:n.941-306T=
XM_011512992.2:c.1154-306T=	XP_011511294.1:n.1154-306T=
XR_001740207.2:n.1391-306T=
XR_001740208.2:n.1391-306T=
XR_001740209.2:n.1361-306T=
XR_001740210.1:n.1221-306T=
XR_002959553.1:n.1391-306T=
XR_002959554.1:n.1391-306T=
XR_241502.3:n.1361-306T=
NM_020166.5:c.1268-306T= MANE Select	NP_064551.3:n.1268-306T=
NM_001293273.2:c.917-306T=	NP_001280202.1:n.917-306T=
NR_120639.2:n.1091-306T=
NR_120640.2:n.1935-306T=