Canonical Allele Identifier: CA1425382923

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183038987A= , CM000665.2:g.183038987A=	GRCh38
NC_000003.11:g.182756775A= , CM000665.1:g.182756775A=	GRCh37
NC_000003.10:g.184239469A=	NCBI36
NG_008100.1:g.65591T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1377+39T= MANE Select	ENSP00000265594.4:n.1377+39T=
ENST00000265594.8:c.1377+39T=	ENSP00000265594.4:n.1377+39T=
ENST00000476176.5:c.1236+39T=	ENSP00000420433.1:n.1236+39T=
ENST00000492597.5:c.1050+39T=	ENSP00000419898.1:n.1050+39T=
ENST00000495767.5:c.*958+39T=	ENSP00000419658.1:n.*958+39T=
ENST00000497830.5:c.*974+39T=	ENSP00000420088.1:n.*974+39T=
ENST00000497959.5:c.1263+39T=	ENSP00000420648.1:n.1263+39T=
ENST00000539926.5:c.927+39T=	ENSP00000441253.2:n.927+39T=
ENST00000610757.4:c.927+39T=	ENSP00000480435.1:n.927+39T=
ENST00000629669.2:c.1263+39T=	ENSP00000486824.1:n.1263+39T=
NM_001293273.1:c.1026+39T=	NP_001280202.1:n.1026+39T=
NM_020166.4:c.1377+39T=	NP_064551.3:n.1377+39T=
NR_120639.1:n.1291+39T=
NR_120640.1:n.2044+39T=
XM_006713702.1:c.1050+39T=	XP_006713765.1:n.1050+39T=
XM_011512992.1:c.1263+39T=	XP_011511294.1:n.1263+39T=
XM_011512993.1:c.1377+39T=	XP_011511295.1:n.1377+39T=
XR_241502.2:n.1524+39T=
XR_924159.1:n.1524+39T=
NM_001363880.1:c.1050+39T=	NP_001350809.1:n.1050+39T=
XM_011512992.2:c.1263+39T=	XP_011511294.1:n.1263+39T=
XR_001740207.2:n.1500+39T=
XR_001740208.2:n.1500+39T=
XR_001740209.2:n.1470+39T=
XR_001740210.1:n.1330+39T=
XR_002959553.1:n.1500+39T=
XR_002959554.1:n.1500+39T=
XR_241502.3:n.1470+39T=
NM_020166.5:c.1377+39T= MANE Select	NP_064551.3:n.1377+39T=
NM_001293273.2:c.1026+39T=	NP_001280202.1:n.1026+39T=
NR_120639.2:n.1200+39T=
NR_120640.2:n.2044+39T=