Canonical Allele Identifier: CA355321812
Gene: MCCC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183039043T>A , CM000665.2:g.183039043T>A GRCh38
NC_000003.11:g.182756831T>A , CM000665.1:g.182756831T>A GRCh37
NC_000003.10:g.184239525T>A NCBI36
NG_008100.1:g.65535A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000265594.9:c.1360A>T MANE Select ENSP00000265594.4:p.Ser454Cys
ENST00000265594.8:c.1360A>T ENSP00000265594.4:p.Ser454Cys
ENST00000476176.5:c.1219A>T ENSP00000420433.1:p.Ser407Cys
ENST00000492597.5:c.1033A>T ENSP00000419898.1:p.Ser345Cys
ENST00000495767.5:c.*941A>T ENSP00000419658.1:n.*941A>T
ENST00000497830.5:c.*957A>T ENSP00000420088.1:n.*957A>T
ENST00000497959.5:c.1246A>T ENSP00000420648.1:p.Ser416Cys
ENST00000539926.5:c.910A>T ENSP00000441253.2:p.Ser304Cys
ENST00000610757.4:c.910A>T ENSP00000480435.1:p.Ser304Cys
ENST00000629669.2:c.1246A>T ENSP00000486824.1:p.Ser416Cys
NM_001293273.1:c.1009A>T NP_001280202.1:p.Ser337Cys
NM_020166.4:c.1360A>T NP_064551.3:p.Ser454Cys
NR_120639.1:n.1274A>T
NR_120640.1:n.2027A>T
XM_006713702.1:c.1033A>T XP_006713765.1:p.Ser345Cys
XM_011512992.1:c.1246A>T XP_011511294.1:p.Ser416Cys
XM_011512993.1:c.1360A>T XP_011511295.1:p.Ser454Cys
XR_241502.2:n.1507A>T
XR_924159.1:n.1507A>T
NM_001363880.1:c.1033A>T NP_001350809.1:p.Ser345Cys
XM_011512992.2:c.1246A>T XP_011511294.1:p.Ser416Cys
XR_001740207.2:n.1483A>T
XR_001740208.2:n.1483A>T
XR_001740209.2:n.1453A>T
XR_001740210.1:n.1313A>T
XR_002959553.1:n.1483A>T
XR_002959554.1:n.1483A>T
XR_241502.3:n.1453A>T
NM_020166.5:c.1360A>T MANE Select NP_064551.3:p.Ser454Cys
NM_001293273.2:c.1009A>T NP_001280202.1:p.Ser337Cys
NR_120639.2:n.1183A>T
NR_120640.2:n.2027A>T