Canonical Allele Identifier: CA2718800

Gene: MCCC1

Linked Data

• dbSNP Id: rs767128340
• ExAC: 3:182756815 T / C
• gnomAD v2: 3-182756815-T-C
• gnomAD v3: 3-183039027-T-C
• gnomAD v4: 3-183039027-T-C
• COSMIC: COSM3719059
• MyVariant Identifiers: chr3:g.182756815T>C (hg19) ; chr3:g.183039027T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039027T>C , CM000665.2:g.183039027T>C	GRCh38
NC_000003.11:g.182756815T>C , CM000665.1:g.182756815T>C	GRCh37
NC_000003.10:g.184239509T>C	NCBI36
NG_008100.1:g.65551A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000265594.9:c.1376A>G MANE Select	ENSP00000265594.4:p.Asn459Ser
ENST00000265594.8:c.1376A>G	ENSP00000265594.4:p.Asn459Ser
ENST00000476176.5:c.1235A>G	ENSP00000420433.1:p.Asn412Ser
ENST00000492597.5:c.1049A>G	ENSP00000419898.1:p.Asn350Ser
ENST00000495767.5:c.*957A>G	ENSP00000419658.1:n.*957A>G
ENST00000497830.5:c.*973A>G	ENSP00000420088.1:n.*973A>G
ENST00000497959.5:c.1262A>G	ENSP00000420648.1:p.Asn421Ser
ENST00000539926.5:c.926A>G	ENSP00000441253.2:p.Asn309Ser
ENST00000610757.4:c.926A>G	ENSP00000480435.1:p.Asn309Ser
ENST00000629669.2:c.1262A>G	ENSP00000486824.1:p.Asn421Ser
NM_001293273.1:c.1025A>G	NP_001280202.1:p.Asn342Ser
NM_020166.4:c.1376A>G	NP_064551.3:p.Asn459Ser
NR_120639.1:n.1290A>G
NR_120640.1:n.2043A>G
XM_006713702.1:c.1049A>G	XP_006713765.1:p.Asn350Ser
XM_011512992.1:c.1262A>G	XP_011511294.1:p.Asn421Ser
XM_011512993.1:c.1376A>G	XP_011511295.1:p.Asn459Ser
XR_241502.2:n.1523A>G
XR_924159.1:n.1523A>G
NM_001363880.1:c.1049A>G	NP_001350809.1:p.Asn350Ser
XM_011512992.2:c.1262A>G	XP_011511294.1:p.Asn421Ser
XR_001740207.2:n.1499A>G
XR_001740208.2:n.1499A>G
XR_001740209.2:n.1469A>G
XR_001740210.1:n.1329A>G
XR_002959553.1:n.1499A>G
XR_002959554.1:n.1499A>G
XR_241502.3:n.1469A>G
NM_020166.5:c.1376A>G MANE Select	NP_064551.3:p.Asn459Ser
NM_001293273.2:c.1025A>G	NP_001280202.1:p.Asn342Ser
NR_120639.2:n.1199A>G
NR_120640.2:n.2043A>G