Canonical Allele Identifier: CA437092785

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182756853C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039065C>G , CM000665.2:g.183039065C>G	GRCh38
NC_000003.11:g.182756853C>G , CM000665.1:g.182756853C>G	GRCh37
NC_000003.10:g.184239547C>G	NCBI36
NG_008100.1:g.65513G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1338G>C MANE Select	ENSP00000265594.4:p.Ala446=
ENST00000265594.8:c.1338G>C	ENSP00000265594.4:p.Ala446=
ENST00000476176.5:c.1197G>C	ENSP00000420433.1:p.Ala399=
ENST00000492597.5:c.1011G>C	ENSP00000419898.1:p.Ala337=
ENST00000495767.5:c.*919G>C	ENSP00000419658.1:n.*919G>C
ENST00000497830.5:c.*935G>C	ENSP00000420088.1:n.*935G>C
ENST00000497959.5:c.1224G>C	ENSP00000420648.1:p.Ala408=
ENST00000539926.5:c.888G>C	ENSP00000441253.2:p.Ala296=
ENST00000610757.4:c.888G>C	ENSP00000480435.1:p.Ala296=
ENST00000629669.2:c.1224G>C	ENSP00000486824.1:p.Ala408=
NM_001293273.1:c.987G>C	NP_001280202.1:p.Ala329=
NM_020166.4:c.1338G>C	NP_064551.3:p.Ala446=
NR_120639.1:n.1252G>C
NR_120640.1:n.2005G>C
XM_006713702.1:c.1011G>C	XP_006713765.1:p.Ala337=
XM_011512992.1:c.1224G>C	XP_011511294.1:p.Ala408=
XM_011512993.1:c.1338G>C	XP_011511295.1:p.Ala446=
XR_241502.2:n.1485G>C
XR_924159.1:n.1485G>C
NM_001363880.1:c.1011G>C	NP_001350809.1:p.Ala337=
XM_011512992.2:c.1224G>C	XP_011511294.1:p.Ala408=
XR_001740207.2:n.1461G>C
XR_001740208.2:n.1461G>C
XR_001740209.2:n.1431G>C
XR_001740210.1:n.1291G>C
XR_002959553.1:n.1461G>C
XR_002959554.1:n.1461G>C
XR_241502.3:n.1431G>C
NM_020166.5:c.1338G>C MANE Select	NP_064551.3:p.Ala446=
NM_001293273.2:c.987G>C	NP_001280202.1:p.Ala329=
NR_120639.2:n.1161G>C
NR_120640.2:n.2005G>C