Canonical Allele Identifier: CA355321667
Community Standard Title: NM_020166.5(MCCC1):c.220C>T (p.Gln74Ter)
Gene: MCCC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183092462G>A , CM000665.2:g.183092462G>A GRCh38
NC_000003.11:g.182810250G>A , CM000665.1:g.182810250G>A GRCh37
NC_000003.10:g.184292944G>A NCBI36
NG_008100.1:g.12116C>T

Transcript Alleles

HGVS Amino-acid Change
NM_020166.5:c.220C>T MANE Select NP_064551.3:p.Gln74Ter
ENST00000265594.9:c.220C>T MANE Select ENSP00000265594.4:p.Gln74Ter
NM_001293273.1:c.44+2097C>T NP_001280202.1:n.44+2097C>T
NM_001293273.2:c.44+2097C>T NP_001280202.1:n.44+2097C>T
NM_001363880.1:c.-55+2097C>T NP_001350809.1:n.-55+2097C>T
NM_020166.4:c.220C>T NP_064551.3:p.Gln74Ter
NR_120639.1:n.283+2097C>T
NR_120639.2:n.192+2097C>T
NR_120640.1:n.887C>T
NR_120640.2:n.887C>T
ENST00000265594.8:c.220C>T ENSP00000265594.4:p.Gln74Ter
ENST00000466650.5:c.136+2097C>T ENSP00000418979.1:n.136+2097C>T
ENST00000473955.1:n.133C>T
ENST00000476176.5:c.136+2097C>T ENSP00000420433.1:n.136+2097C>T
ENST00000486226.1:c.220C>T ENSP00000420223.1:p.Gln74Ter
ENST00000487634.5:c.136+2097C>T ENSP00000420591.1:n.136+2097C>T
ENST00000490284.5:c.89+6890C>T ENSP00000419328.1:n.89+6890C>T
ENST00000492597.5:c.-55+2097C>T ENSP00000419898.1:n.-55+2097C>T
ENST00000495767.5:c.136+2097C>T ENSP00000419658.1:n.136+2097C>T
ENST00000497830.5:c.136+2097C>T ENSP00000420088.1:n.136+2097C>T
ENST00000497959.5:c.106C>T ENSP00000420648.1:p.Gln36Ter
ENST00000539926.5:c.-55+2097C>T ENSP00000441253.2:n.-55+2097C>T
ENST00000610757.4:c.-108C>T ENSP00000480435.1:n.-108C>T
ENST00000629669.2:c.106C>T ENSP00000486824.1:p.Gln36Ter
XM_006713702.1:c.-55+2097C>T XP_006713765.1:n.-55+2097C>T
XM_011512992.1:c.106C>T XP_011511294.1:p.Gln36Ter
XM_011512992.2:c.106C>T XP_011511294.1:p.Gln36Ter
XM_011512993.1:c.220C>T XP_011511295.1:p.Gln74Ter
XR_001740207.2:n.343C>T
XR_001740208.2:n.343C>T
XR_001740209.2:n.313C>T
XR_001740210.1:n.226+2097C>T
XR_002959553.1:n.343C>T
XR_002959554.1:n.343C>T
XR_241502.2:n.367C>T
XR_241502.3:n.313C>T
XR_924159.1:n.367C>T