Canonical Allele Identifier: CA312677

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039072C>T , CM000665.2:g.183039072C>T	GRCh38
NC_000003.11:g.182756860C>T , CM000665.1:g.182756860C>T	GRCh37
NC_000003.10:g.184239554C>T	NCBI36
NG_008100.1:g.65506G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.1331G>A MANE Select	NP_064551.3:p.Arg444His
ENST00000265594.9:c.1331G>A MANE Select	ENSP00000265594.4:p.Arg444His
NM_001293273.1:c.980G>A	NP_001280202.1:p.Arg327His
NM_001293273.2:c.980G>A	NP_001280202.1:p.Arg327His
NM_001363880.1:c.1004G>A	NP_001350809.1:p.Arg335His
NM_020166.4:c.1331G>A	NP_064551.3:p.Arg444His
NR_120639.1:n.1245G>A
NR_120639.2:n.1154G>A
NR_120640.1:n.1998G>A
NR_120640.2:n.1998G>A
ENST00000265594.8:c.1331G>A	ENSP00000265594.4:p.Arg444His
ENST00000476176.5:c.1190G>A	ENSP00000420433.1:p.Arg397His
ENST00000492597.5:c.1004G>A	ENSP00000419898.1:p.Arg335His
ENST00000495767.5:c.*912G>A	ENSP00000419658.1:n.*912G>A
ENST00000497830.5:c.*928G>A	ENSP00000420088.1:n.*928G>A
ENST00000497959.5:c.1217G>A	ENSP00000420648.1:p.Arg406His
ENST00000539926.5:c.881G>A	ENSP00000441253.2:p.Arg294His
ENST00000610757.4:c.881G>A	ENSP00000480435.1:p.Arg294His
ENST00000629669.2:c.1217G>A	ENSP00000486824.1:p.Arg406His
XM_006713702.1:c.1004G>A	XP_006713765.1:p.Arg335His
XM_011512992.1:c.1217G>A	XP_011511294.1:p.Arg406His
XM_011512992.2:c.1217G>A	XP_011511294.1:p.Arg406His
XM_011512993.1:c.1331G>A	XP_011511295.1:p.Arg444His
XR_001740207.2:n.1454G>A
XR_001740208.2:n.1454G>A
XR_001740209.2:n.1424G>A
XR_001740210.1:n.1284G>A
XR_002959553.1:n.1454G>A
XR_002959554.1:n.1454G>A
XR_241502.2:n.1478G>A
XR_241502.3:n.1424G>A
XR_924159.1:n.1478G>A