Canonical Allele Identifier: CA903589255
Gene: MCCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1202429707

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183039220T>G , CM000665.2:g.183039220T>G GRCh38
NC_000003.11:g.182757008T>G , CM000665.1:g.182757008T>G GRCh37
NC_000003.10:g.184239702T>G NCBI36
NG_008100.1:g.65358A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000265594.9:c.1268-85A>C MANE Select ENSP00000265594.4:n.1268-85A>C
ENST00000265594.8:c.1268-85A>C ENSP00000265594.4:n.1268-85A>C
ENST00000476176.5:c.1127-85A>C ENSP00000420433.1:n.1127-85A>C
ENST00000492597.5:c.941-85A>C ENSP00000419898.1:n.941-85A>C
ENST00000495767.5:c.*849-85A>C ENSP00000419658.1:n.*849-85A>C
ENST00000497830.5:c.*865-85A>C ENSP00000420088.1:n.*865-85A>C
ENST00000497959.5:c.1154-85A>C ENSP00000420648.1:n.1154-85A>C
ENST00000539926.5:c.818-85A>C ENSP00000441253.2:n.818-85A>C
ENST00000610757.4:c.818-85A>C ENSP00000480435.1:n.818-85A>C
ENST00000629669.2:c.1154-85A>C ENSP00000486824.1:n.1154-85A>C
NM_001293273.1:c.917-85A>C NP_001280202.1:n.917-85A>C
NM_020166.4:c.1268-85A>C NP_064551.3:n.1268-85A>C
NR_120639.1:n.1182-85A>C
NR_120640.1:n.1935-85A>C
XM_006713702.1:c.941-85A>C XP_006713765.1:n.941-85A>C
XM_011512992.1:c.1154-85A>C XP_011511294.1:n.1154-85A>C
XM_011512993.1:c.1268-85A>C XP_011511295.1:n.1268-85A>C
XR_241502.2:n.1415-85A>C
XR_924159.1:n.1415-85A>C
NM_001363880.1:c.941-85A>C NP_001350809.1:n.941-85A>C
XM_011512992.2:c.1154-85A>C XP_011511294.1:n.1154-85A>C
XR_001740207.2:n.1391-85A>C
XR_001740208.2:n.1391-85A>C
XR_001740209.2:n.1361-85A>C
XR_001740210.1:n.1221-85A>C
XR_002959553.1:n.1391-85A>C
XR_002959554.1:n.1391-85A>C
XR_241502.3:n.1361-85A>C
NM_020166.5:c.1268-85A>C MANE Select NP_064551.3:n.1268-85A>C
NM_001293273.2:c.917-85A>C NP_001280202.1:n.917-85A>C
NR_120639.2:n.1091-85A>C
NR_120640.2:n.1935-85A>C