Canonical Allele Identifier: CA1425382213

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037258C= , CM000665.2:g.183037258C=	GRCh38
NC_000003.11:g.182755046C= , CM000665.1:g.182755046C=	GRCh37
NC_000003.10:g.184237740C=	NCBI36
NG_008100.1:g.67320G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1554G= MANE Select	ENSP00000265594.4:p.Lys518=
ENST00000265594.8:c.1554G=	ENSP00000265594.4:p.Lys518=
ENST00000476176.5:c.1413G=	ENSP00000420433.1:p.Lys471=
ENST00000489909.1:n.98G=
ENST00000492597.5:c.1227G=	ENSP00000419898.1:p.Lys409=
ENST00000495767.5:c.*1135G=	ENSP00000419658.1:n.*1135G=
ENST00000497830.5:c.*1151G=	ENSP00000420088.1:n.*1151G=
ENST00000497959.5:c.1263+1768G=	ENSP00000420648.1:n.1263+1768G=
ENST00000539926.5:c.1104G=	ENSP00000441253.2:p.Lys368=
ENST00000610757.4:c.1104G=	ENSP00000480435.1:p.Lys368=
ENST00000629669.2:c.1263+1768G=	ENSP00000486824.1:n.1263+1768G=
NM_001293273.1:c.1203G=	NP_001280202.1:p.Lys401=
NM_020166.4:c.1554G=	NP_064551.3:p.Lys518=
NR_120639.1:n.1468G=
NR_120640.1:n.2044+1768G=
XM_006713702.1:c.1227G=	XP_006713765.1:p.Lys409=
XM_011512992.1:c.1440G=	XP_011511294.1:p.Lys480=
XM_011512993.1:c.1377+1768G=	XP_011511295.1:n.1377+1768G=
XR_241502.2:n.1524+1768G=
XR_924159.1:n.1701G=
NM_001363880.1:c.1227G=	NP_001350809.1:p.Lys409=
XM_011512992.2:c.1440G=	XP_011511294.1:p.Lys480=
XR_001740207.2:n.1677G=
XR_001740208.2:n.1677G=
XR_001740209.2:n.1470+1768G=
XR_001740210.1:n.1507G=
XR_002959553.1:n.1677G=
XR_002959554.1:n.1500+1768G=
XR_241502.3:n.1470+1768G=
NM_020166.5:c.1554G= MANE Select	NP_064551.3:p.Lys518=
NM_001293273.2:c.1203G=	NP_001280202.1:p.Lys401=
NR_120639.2:n.1377G=
NR_120640.2:n.2044+1768G=