Canonical Allele Identifier: CA355331431

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183072475C>G , CM000665.2:g.183072475C>G	GRCh38
NC_000003.11:g.182790263C>G , CM000665.1:g.182790263C>G	GRCh37
NC_000003.10:g.184272957C>G	NCBI36
NG_008100.1:g.32103G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.382G>C MANE Select	NP_064551.3:p.Gly128Arg
ENST00000265594.9:c.382G>C MANE Select	ENSP00000265594.4:p.Gly128Arg
NM_001293273.1:c.141-1118G>C	NP_001280202.1:n.141-1118G>C
NM_001293273.2:c.141-1118G>C	NP_001280202.1:n.141-1118G>C
NM_001363880.1:c.55G>C	NP_001350809.1:p.Gly19Arg
NM_020166.4:c.382G>C	NP_064551.3:p.Gly128Arg
NR_120639.1:n.296G>C
NR_120639.2:n.205G>C
NR_120640.1:n.1049G>C
NR_120640.2:n.1049G>C
ENST00000265594.8:c.382G>C	ENSP00000265594.4:p.Gly128Arg
ENST00000466650.5:c.*89-1118G>C	ENSP00000418979.1:n.*89-1118G>C
ENST00000476176.5:c.241G>C	ENSP00000420433.1:p.Gly81Arg
ENST00000486226.1:c.*139G>C	ENSP00000420223.1:n.*139G>C
ENST00000487634.5:c.149G>C	ENSP00000420591.1:p.Arg50Thr
ENST00000490284.5:c.102G>C	ENSP00000419328.1:p.Gln34His
ENST00000492597.5:c.55G>C	ENSP00000419898.1:p.Gly19Arg
ENST00000495767.5:c.149G>C	ENSP00000419658.1:p.Arg50Thr
ENST00000497830.5:c.*89-1118G>C	ENSP00000420088.1:n.*89-1118G>C
ENST00000497959.5:c.268G>C	ENSP00000420648.1:p.Gly90Arg
ENST00000539926.5:c.43-1118G>C	ENSP00000441253.2:n.43-1118G>C
ENST00000610757.4:c.43-1118G>C	ENSP00000480435.1:n.43-1118G>C
ENST00000629669.2:c.268G>C	ENSP00000486824.1:p.Gly90Arg
XM_006713702.1:c.55G>C	XP_006713765.1:p.Gly19Arg
XM_011512992.1:c.268G>C	XP_011511294.1:p.Gly90Arg
XM_011512992.2:c.268G>C	XP_011511294.1:p.Gly90Arg
XM_011512993.1:c.382G>C	XP_011511295.1:p.Gly128Arg
XR_001740207.2:n.505G>C
XR_001740208.2:n.505G>C
XR_001740209.2:n.475G>C
XR_001740210.1:n.335G>C
XR_002959553.1:n.505G>C
XR_002959554.1:n.505G>C
XR_241502.2:n.529G>C
XR_241502.3:n.475G>C
XR_924159.1:n.529G>C