Canonical Allele Identifier: CA355321906

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182756855C>T (hg19) ; chr3:g.183039067C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039067C>T , CM000665.2:g.183039067C>T	GRCh38
NC_000003.11:g.182756855C>T , CM000665.1:g.182756855C>T	GRCh37
NC_000003.10:g.184239549C>T	NCBI36
NG_008100.1:g.65511G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1336G>A MANE Select	ENSP00000265594.4:p.Ala446Thr
ENST00000265594.8:c.1336G>A	ENSP00000265594.4:p.Ala446Thr
ENST00000476176.5:c.1195G>A	ENSP00000420433.1:p.Ala399Thr
ENST00000492597.5:c.1009G>A	ENSP00000419898.1:p.Ala337Thr
ENST00000495767.5:c.*917G>A	ENSP00000419658.1:n.*917G>A
ENST00000497830.5:c.*933G>A	ENSP00000420088.1:n.*933G>A
ENST00000497959.5:c.1222G>A	ENSP00000420648.1:p.Ala408Thr
ENST00000539926.5:c.886G>A	ENSP00000441253.2:p.Ala296Thr
ENST00000610757.4:c.886G>A	ENSP00000480435.1:p.Ala296Thr
ENST00000629669.2:c.1222G>A	ENSP00000486824.1:p.Ala408Thr
NM_001293273.1:c.985G>A	NP_001280202.1:p.Ala329Thr
NM_020166.4:c.1336G>A	NP_064551.3:p.Ala446Thr
NR_120639.1:n.1250G>A
NR_120640.1:n.2003G>A
XM_006713702.1:c.1009G>A	XP_006713765.1:p.Ala337Thr
XM_011512992.1:c.1222G>A	XP_011511294.1:p.Ala408Thr
XM_011512993.1:c.1336G>A	XP_011511295.1:p.Ala446Thr
XR_241502.2:n.1483G>A
XR_924159.1:n.1483G>A
NM_001363880.1:c.1009G>A	NP_001350809.1:p.Ala337Thr
XM_011512992.2:c.1222G>A	XP_011511294.1:p.Ala408Thr
XR_001740207.2:n.1459G>A
XR_001740208.2:n.1459G>A
XR_001740209.2:n.1429G>A
XR_001740210.1:n.1289G>A
XR_002959553.1:n.1459G>A
XR_002959554.1:n.1459G>A
XR_241502.3:n.1429G>A
NM_020166.5:c.1336G>A MANE Select	NP_064551.3:p.Ala446Thr
NM_001293273.2:c.985G>A	NP_001280202.1:p.Ala329Thr
NR_120639.2:n.1159G>A
NR_120640.2:n.2003G>A