Canonical Allele Identifier: CA437092800

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182756868T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039080T>G , CM000665.2:g.183039080T>G	GRCh38
NC_000003.11:g.182756868T>G , CM000665.1:g.182756868T>G	GRCh37
NC_000003.10:g.184239562T>G	NCBI36
NG_008100.1:g.65498A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1323A>C MANE Select	ENSP00000265594.4:p.Ala441=
ENST00000265594.8:c.1323A>C	ENSP00000265594.4:p.Ala441=
ENST00000476176.5:c.1182A>C	ENSP00000420433.1:p.Ala394=
ENST00000492597.5:c.996A>C	ENSP00000419898.1:p.Ala332=
ENST00000495767.5:c.*904A>C	ENSP00000419658.1:n.*904A>C
ENST00000497830.5:c.*920A>C	ENSP00000420088.1:n.*920A>C
ENST00000497959.5:c.1209A>C	ENSP00000420648.1:p.Ala403=
ENST00000539926.5:c.873A>C	ENSP00000441253.2:p.Ala291=
ENST00000610757.4:c.873A>C	ENSP00000480435.1:p.Ala291=
ENST00000629669.2:c.1209A>C	ENSP00000486824.1:p.Ala403=
NM_001293273.1:c.972A>C	NP_001280202.1:p.Ala324=
NM_020166.4:c.1323A>C	NP_064551.3:p.Ala441=
NR_120639.1:n.1237A>C
NR_120640.1:n.1990A>C
XM_006713702.1:c.996A>C	XP_006713765.1:p.Ala332=
XM_011512992.1:c.1209A>C	XP_011511294.1:p.Ala403=
XM_011512993.1:c.1323A>C	XP_011511295.1:p.Ala441=
XR_241502.2:n.1470A>C
XR_924159.1:n.1470A>C
NM_001363880.1:c.996A>C	NP_001350809.1:p.Ala332=
XM_011512992.2:c.1209A>C	XP_011511294.1:p.Ala403=
XR_001740207.2:n.1446A>C
XR_001740208.2:n.1446A>C
XR_001740209.2:n.1416A>C
XR_001740210.1:n.1276A>C
XR_002959553.1:n.1446A>C
XR_002959554.1:n.1446A>C
XR_241502.3:n.1416A>C
NM_020166.5:c.1323A>C MANE Select	NP_064551.3:p.Ala441=
NM_001293273.2:c.972A>C	NP_001280202.1:p.Ala324=
NR_120639.2:n.1146A>C
NR_120640.2:n.1990A>C