Canonical Allele Identifier: CA355319775

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182755007A>C (hg19) ; chr3:g.183037219A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037219A>C , CM000665.2:g.183037219A>C	GRCh38
NC_000003.11:g.182755007A>C , CM000665.1:g.182755007A>C	GRCh37
NC_000003.10:g.184237701A>C	NCBI36
NG_008100.1:g.67359T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1593T>G MANE Select	ENSP00000265594.4:p.His531Gln
ENST00000265594.8:c.1593T>G	ENSP00000265594.4:p.His531Gln
ENST00000476176.5:c.1452T>G	ENSP00000420433.1:p.His484Gln
ENST00000489909.1:n.137T>G
ENST00000492597.5:c.1266T>G	ENSP00000419898.1:p.His422Gln
ENST00000495767.5:c.*1174T>G	ENSP00000419658.1:n.*1174T>G
ENST00000497830.5:c.*1190T>G	ENSP00000420088.1:n.*1190T>G
ENST00000497959.5:c.1263+1807T>G	ENSP00000420648.1:n.1263+1807T>G
ENST00000539926.5:c.1143T>G	ENSP00000441253.2:p.His381Gln
ENST00000610757.4:c.1143T>G	ENSP00000480435.1:p.His381Gln
ENST00000629669.2:c.1263+1807T>G	ENSP00000486824.1:n.1263+1807T>G
NM_001293273.1:c.1242T>G	NP_001280202.1:p.His414Gln
NM_020166.4:c.1593T>G	NP_064551.3:p.His531Gln
NR_120639.1:n.1507T>G
NR_120640.1:n.2044+1807T>G
XM_006713702.1:c.1266T>G	XP_006713765.1:p.His422Gln
XM_011512992.1:c.1479T>G	XP_011511294.1:p.His493Gln
XM_011512993.1:c.1377+1807T>G	XP_011511295.1:n.1377+1807T>G
XR_241502.2:n.1524+1807T>G
XR_924159.1:n.1740T>G
NM_001363880.1:c.1266T>G	NP_001350809.1:p.His422Gln
XM_011512992.2:c.1479T>G	XP_011511294.1:p.His493Gln
XR_001740207.2:n.1716T>G
XR_001740208.2:n.1716T>G
XR_001740209.2:n.1470+1807T>G
XR_001740210.1:n.1546T>G
XR_002959553.1:n.1716T>G
XR_002959554.1:n.1500+1807T>G
XR_241502.3:n.1470+1807T>G
NM_020166.5:c.1593T>G MANE Select	NP_064551.3:p.His531Gln
NM_001293273.2:c.1242T>G	NP_001280202.1:p.His414Gln
NR_120639.2:n.1416T>G
NR_120640.2:n.2044+1807T>G