Canonical Allele Identifier: CA2718811

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039073G>A , CM000665.2:g.183039073G>A	GRCh38
NC_000003.11:g.182756861G>A , CM000665.1:g.182756861G>A	GRCh37
NC_000003.10:g.184239555G>A	NCBI36
NG_008100.1:g.65505C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.1330C>T MANE Select	NP_064551.3:p.Arg444Cys
ENST00000265594.9:c.1330C>T MANE Select	ENSP00000265594.4:p.Arg444Cys
NM_001293273.1:c.979C>T	NP_001280202.1:p.Arg327Cys
NM_001293273.2:c.979C>T	NP_001280202.1:p.Arg327Cys
NM_001363880.1:c.1003C>T	NP_001350809.1:p.Arg335Cys
NM_020166.4:c.1330C>T	NP_064551.3:p.Arg444Cys
NR_120639.1:n.1244C>T
NR_120639.2:n.1153C>T
NR_120640.1:n.1997C>T
NR_120640.2:n.1997C>T
ENST00000265594.8:c.1330C>T	ENSP00000265594.4:p.Arg444Cys
ENST00000476176.5:c.1189C>T	ENSP00000420433.1:p.Arg397Cys
ENST00000492597.5:c.1003C>T	ENSP00000419898.1:p.Arg335Cys
ENST00000495767.5:c.*911C>T	ENSP00000419658.1:n.*911C>T
ENST00000497830.5:c.*927C>T	ENSP00000420088.1:n.*927C>T
ENST00000497959.5:c.1216C>T	ENSP00000420648.1:p.Arg406Cys
ENST00000539926.5:c.880C>T	ENSP00000441253.2:p.Arg294Cys
ENST00000610757.4:c.880C>T	ENSP00000480435.1:p.Arg294Cys
ENST00000629669.2:c.1216C>T	ENSP00000486824.1:p.Arg406Cys
XM_006713702.1:c.1003C>T	XP_006713765.1:p.Arg335Cys
XM_011512992.1:c.1216C>T	XP_011511294.1:p.Arg406Cys
XM_011512992.2:c.1216C>T	XP_011511294.1:p.Arg406Cys
XM_011512993.1:c.1330C>T	XP_011511295.1:p.Arg444Cys
XR_001740207.2:n.1453C>T
XR_001740208.2:n.1453C>T
XR_001740209.2:n.1423C>T
XR_001740210.1:n.1283C>T
XR_002959553.1:n.1453C>T
XR_002959554.1:n.1453C>T
XR_241502.2:n.1477C>T
XR_241502.3:n.1423C>T
XR_924159.1:n.1477C>T