Canonical Allele Identifier: CA1425384262
Gene: MCCC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183042120T= , CM000665.2:g.183042120T= GRCh38
NC_000003.11:g.182759908T= , CM000665.1:g.182759908T= GRCh37
NC_000003.10:g.184242602T= NCBI36
NG_008100.1:g.62458A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265594.9:c.1084-370A= MANE Select ENSP00000265594.4:n.1084-370A=
ENST00000265594.8:c.1084-370A= ENSP00000265594.4:n.1084-370A=
ENST00000476176.5:c.943-370A= ENSP00000420433.1:n.943-370A=
ENST00000492597.5:c.757-370A= ENSP00000419898.1:n.757-370A=
ENST00000495767.5:c.*665-370A= ENSP00000419658.1:n.*665-370A=
ENST00000497830.5:c.*681-370A= ENSP00000420088.1:n.*681-370A=
ENST00000497959.5:c.970-370A= ENSP00000420648.1:n.970-370A=
ENST00000539926.5:c.634-370A= ENSP00000441253.2:n.634-370A=
ENST00000610757.4:c.634-370A= ENSP00000480435.1:n.634-370A=
ENST00000629669.2:c.970-370A= ENSP00000486824.1:n.970-370A=
NM_001293273.1:c.733-370A= NP_001280202.1:n.733-370A=
NM_020166.4:c.1084-370A= NP_064551.3:n.1084-370A=
NR_120639.1:n.998-370A=
NR_120640.1:n.1751-370A=
XM_006713702.1:c.757-370A= XP_006713765.1:n.757-370A=
XM_011512992.1:c.970-370A= XP_011511294.1:n.970-370A=
XM_011512993.1:c.1084-370A= XP_011511295.1:n.1084-370A=
XR_241502.2:n.1231-370A=
XR_924159.1:n.1231-370A=
NM_001363880.1:c.757-370A= NP_001350809.1:n.757-370A=
XM_011512992.2:c.970-370A= XP_011511294.1:n.970-370A=
XR_001740207.2:n.1207-370A=
XR_001740208.2:n.1207-370A=
XR_001740209.2:n.1177-370A=
XR_001740210.1:n.1037-370A=
XR_002959553.1:n.1207-370A=
XR_002959554.1:n.1207-370A=
XR_241502.3:n.1177-370A=
NM_020166.5:c.1084-370A= MANE Select NP_064551.3:n.1084-370A=
NM_001293273.2:c.733-370A= NP_001280202.1:n.733-370A=
NR_120639.2:n.907-370A=
NR_120640.2:n.1751-370A=