Canonical Allele Identifier: CA1425383988

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183041480T= , CM000665.2:g.183041480T=	GRCh38
NC_000003.11:g.182759268T= , CM000665.1:g.182759268T=	GRCh37
NC_000003.10:g.184241962T=	NCBI36
NG_008100.1:g.63098A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1267+87A= MANE Select	ENSP00000265594.4:n.1267+87A=
ENST00000265594.8:c.1267+87A=	ENSP00000265594.4:n.1267+87A=
ENST00000476176.5:c.1126+87A=	ENSP00000420433.1:n.1126+87A=
ENST00000492597.5:c.940+87A=	ENSP00000419898.1:n.940+87A=
ENST00000495767.5:c.*848+87A=	ENSP00000419658.1:n.*848+87A=
ENST00000497830.5:c.*864+87A=	ENSP00000420088.1:n.*864+87A=
ENST00000497959.5:c.1153+87A=	ENSP00000420648.1:n.1153+87A=
ENST00000539926.5:c.817+87A=	ENSP00000441253.2:n.817+87A=
ENST00000610757.4:c.817+87A=	ENSP00000480435.1:n.817+87A=
ENST00000629669.2:c.1153+87A=	ENSP00000486824.1:n.1153+87A=
NM_001293273.1:c.916+87A=	NP_001280202.1:n.916+87A=
NM_020166.4:c.1267+87A=	NP_064551.3:n.1267+87A=
NR_120639.1:n.1181+87A=
NR_120640.1:n.1934+87A=
XM_006713702.1:c.940+87A=	XP_006713765.1:n.940+87A=
XM_011512992.1:c.1153+87A=	XP_011511294.1:n.1153+87A=
XM_011512993.1:c.1267+87A=	XP_011511295.1:n.1267+87A=
XR_241502.2:n.1414+87A=
XR_924159.1:n.1414+87A=
NM_001363880.1:c.940+87A=	NP_001350809.1:n.940+87A=
XM_011512992.2:c.1153+87A=	XP_011511294.1:n.1153+87A=
XR_001740207.2:n.1390+87A=
XR_001740208.2:n.1390+87A=
XR_001740209.2:n.1360+87A=
XR_001740210.1:n.1220+87A=
XR_002959553.1:n.1390+87A=
XR_002959554.1:n.1390+87A=
XR_241502.3:n.1360+87A=
NM_020166.5:c.1267+87A= MANE Select	NP_064551.3:n.1267+87A=
NM_001293273.2:c.916+87A=	NP_001280202.1:n.916+87A=
NR_120639.2:n.1090+87A=
NR_120640.2:n.1934+87A=