Canonical Allele Identifier: CA355321959

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182756870C>T (hg19) ; chr3:g.183039082C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039082C>T , CM000665.2:g.183039082C>T	GRCh38
NC_000003.11:g.182756870C>T , CM000665.1:g.182756870C>T	GRCh37
NC_000003.10:g.184239564C>T	NCBI36
NG_008100.1:g.65496G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1321G>A MANE Select	ENSP00000265594.4:p.Ala441Thr
ENST00000265594.8:c.1321G>A	ENSP00000265594.4:p.Ala441Thr
ENST00000476176.5:c.1180G>A	ENSP00000420433.1:p.Ala394Thr
ENST00000492597.5:c.994G>A	ENSP00000419898.1:p.Ala332Thr
ENST00000495767.5:c.*902G>A	ENSP00000419658.1:n.*902G>A
ENST00000497830.5:c.*918G>A	ENSP00000420088.1:n.*918G>A
ENST00000497959.5:c.1207G>A	ENSP00000420648.1:p.Ala403Thr
ENST00000539926.5:c.871G>A	ENSP00000441253.2:p.Ala291Thr
ENST00000610757.4:c.871G>A	ENSP00000480435.1:p.Ala291Thr
ENST00000629669.2:c.1207G>A	ENSP00000486824.1:p.Ala403Thr
NM_001293273.1:c.970G>A	NP_001280202.1:p.Ala324Thr
NM_020166.4:c.1321G>A	NP_064551.3:p.Ala441Thr
NR_120639.1:n.1235G>A
NR_120640.1:n.1988G>A
XM_006713702.1:c.994G>A	XP_006713765.1:p.Ala332Thr
XM_011512992.1:c.1207G>A	XP_011511294.1:p.Ala403Thr
XM_011512993.1:c.1321G>A	XP_011511295.1:p.Ala441Thr
XR_241502.2:n.1468G>A
XR_924159.1:n.1468G>A
NM_001363880.1:c.994G>A	NP_001350809.1:p.Ala332Thr
XM_011512992.2:c.1207G>A	XP_011511294.1:p.Ala403Thr
XR_001740207.2:n.1444G>A
XR_001740208.2:n.1444G>A
XR_001740209.2:n.1414G>A
XR_001740210.1:n.1274G>A
XR_002959553.1:n.1444G>A
XR_002959554.1:n.1444G>A
XR_241502.3:n.1414G>A
NM_020166.5:c.1321G>A MANE Select	NP_064551.3:p.Ala441Thr
NM_001293273.2:c.970G>A	NP_001280202.1:p.Ala324Thr
NR_120639.2:n.1144G>A
NR_120640.2:n.1988G>A