Canonical Allele Identifier: CA355319982
Gene: MCCC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183037254T>A , CM000665.2:g.183037254T>A GRCh38
NC_000003.11:g.182755042T>A , CM000665.1:g.182755042T>A GRCh37
NC_000003.10:g.184237736T>A NCBI36
NG_008100.1:g.67324A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265594.9:c.1558A>T MANE Select ENSP00000265594.4:p.Lys520Ter
ENST00000265594.8:c.1558A>T ENSP00000265594.4:p.Lys520Ter
ENST00000476176.5:c.1417A>T ENSP00000420433.1:p.Lys473Ter
ENST00000489909.1:n.102A>T
ENST00000492597.5:c.1231A>T ENSP00000419898.1:p.Lys411Ter
ENST00000495767.5:c.*1139A>T ENSP00000419658.1:n.*1139A>T
ENST00000497830.5:c.*1155A>T ENSP00000420088.1:n.*1155A>T
ENST00000497959.5:c.1263+1772A>T ENSP00000420648.1:n.1263+1772A>T
ENST00000539926.5:c.1108A>T ENSP00000441253.2:p.Lys370Ter
ENST00000610757.4:c.1108A>T ENSP00000480435.1:p.Lys370Ter
ENST00000629669.2:c.1263+1772A>T ENSP00000486824.1:n.1263+1772A>T
NM_001293273.1:c.1207A>T NP_001280202.1:p.Lys403Ter
NM_020166.4:c.1558A>T NP_064551.3:p.Lys520Ter
NR_120639.1:n.1472A>T
NR_120640.1:n.2044+1772A>T
XM_006713702.1:c.1231A>T XP_006713765.1:p.Lys411Ter
XM_011512992.1:c.1444A>T XP_011511294.1:p.Lys482Ter
XM_011512993.1:c.1377+1772A>T XP_011511295.1:n.1377+1772A>T
XR_241502.2:n.1524+1772A>T
XR_924159.1:n.1705A>T
NM_001363880.1:c.1231A>T NP_001350809.1:p.Lys411Ter
XM_011512992.2:c.1444A>T XP_011511294.1:p.Lys482Ter
XR_001740207.2:n.1681A>T
XR_001740208.2:n.1681A>T
XR_001740209.2:n.1470+1772A>T
XR_001740210.1:n.1511A>T
XR_002959553.1:n.1681A>T
XR_002959554.1:n.1500+1772A>T
XR_241502.3:n.1470+1772A>T
NM_020166.5:c.1558A>T MANE Select NP_064551.3:p.Lys520Ter
NM_001293273.2:c.1207A>T NP_001280202.1:p.Lys403Ter
NR_120639.2:n.1381A>T
NR_120640.2:n.2044+1772A>T