Canonical Allele Identifier: CA355322067
Gene: MCCC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183039130C>A , CM000665.2:g.183039130C>A GRCh38
NC_000003.11:g.182756918C>A , CM000665.1:g.182756918C>A GRCh37
NC_000003.10:g.184239612C>A NCBI36
NG_008100.1:g.65448G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000265594.9:c.1273G>T MANE Select ENSP00000265594.4:p.Glu425Ter
ENST00000265594.8:c.1273G>T ENSP00000265594.4:p.Glu425Ter
ENST00000476176.5:c.1132G>T ENSP00000420433.1:p.Glu378Ter
ENST00000492597.5:c.946G>T ENSP00000419898.1:p.Glu316Ter
ENST00000495767.5:c.*854G>T ENSP00000419658.1:n.*854G>T
ENST00000497830.5:c.*870G>T ENSP00000420088.1:n.*870G>T
ENST00000497959.5:c.1159G>T ENSP00000420648.1:p.Glu387Ter
ENST00000539926.5:c.823G>T ENSP00000441253.2:p.Glu275Ter
ENST00000610757.4:c.823G>T ENSP00000480435.1:p.Glu275Ter
ENST00000629669.2:c.1159G>T ENSP00000486824.1:p.Glu387Ter
NM_001293273.1:c.922G>T NP_001280202.1:p.Glu308Ter
NM_020166.4:c.1273G>T NP_064551.3:p.Glu425Ter
NR_120639.1:n.1187G>T
NR_120640.1:n.1940G>T
XM_006713702.1:c.946G>T XP_006713765.1:p.Glu316Ter
XM_011512992.1:c.1159G>T XP_011511294.1:p.Glu387Ter
XM_011512993.1:c.1273G>T XP_011511295.1:p.Glu425Ter
XR_241502.2:n.1420G>T
XR_924159.1:n.1420G>T
NM_001363880.1:c.946G>T NP_001350809.1:p.Glu316Ter
XM_011512992.2:c.1159G>T XP_011511294.1:p.Glu387Ter
XR_001740207.2:n.1396G>T
XR_001740208.2:n.1396G>T
XR_001740209.2:n.1366G>T
XR_001740210.1:n.1226G>T
XR_002959553.1:n.1396G>T
XR_002959554.1:n.1396G>T
XR_241502.3:n.1366G>T
NM_020166.5:c.1273G>T MANE Select NP_064551.3:p.Glu425Ter
NM_001293273.2:c.922G>T NP_001280202.1:p.Glu308Ter
NR_120639.2:n.1096G>T
NR_120640.2:n.1940G>T