Canonical Allele Identifier: CA2554044003
Gene: MCCC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183042242_183042243insAAAAGCAAAAGCTGAAAATCAGTGCAAAAGAGGAAGGGGAGA , CM000665.2:g.183042242_183042243insAAAAGCAAAAGCTGAAAATCAGTGCAAAAGAGGAAGGGGAGA GRCh38
NC_000003.11:g.182760030_182760031insAAAAGCAAAAGCTGAAAATCAGTGCAAAAGAGGAAGGGGAGA , CM000665.1:g.182760030_182760031insAAAAGCAAAAGCTGAAAATCAGTGCAAAAGAGGAAGGGGAGA GRCh37
NC_000003.10:g.184242724_184242725insAAAAGCAAAAGCTGAAAATCAGTGCAAAAGAGGAAGGGGAGA NCBI36
NG_008100.1:g.62336_62337insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000265594.9:c.1084-492_1084-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT MANE Select ENSP00000265594.4:n.1084-492_1084-491insCTCCCCTTCCTCTTTTGCACT...
ENST00000265594.8:c.1084-492_1084-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT ENSP00000265594.4:n.1084-492_1084-491insCTCCCCTTCCTCTTTTGCACT...
ENST00000476176.5:c.943-492_943-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT ENSP00000420433.1:n.943-492_943-491insCTCCCCTTCCTCTTTTGCACTGA...
ENST00000492597.5:c.757-492_757-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT ENSP00000419898.1:n.757-492_757-491insCTCCCCTTCCTCTTTTGCACTGA...
ENST00000495767.5:c.*665-492_*665-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT ENSP00000419658.1:n.*665-492_*665-491insCTCCCCTTCCTCTTTTGCACT...
ENST00000497830.5:c.*681-492_*681-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT ENSP00000420088.1:n.*681-492_*681-491insCTCCCCTTCCTCTTTTGCACT...
ENST00000497959.5:c.970-492_970-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT ENSP00000420648.1:n.970-492_970-491insCTCCCCTTCCTCTTTTGCACTGA...
ENST00000539926.5:c.634-492_634-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT ENSP00000441253.2:n.634-492_634-491insCTCCCCTTCCTCTTTTGCACTGA...
ENST00000610757.4:c.634-492_634-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT ENSP00000480435.1:n.634-492_634-491insCTCCCCTTCCTCTTTTGCACTGA...
ENST00000629669.2:c.970-492_970-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT ENSP00000486824.1:n.970-492_970-491insCTCCCCTTCCTCTTTTGCACTGA...
NM_001293273.1:c.733-492_733-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT NP_001280202.1:n.733-492_733-491insCTCCCCTTCCTCTTTTGCACTGATTT...
NM_020166.4:c.1084-492_1084-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT NP_064551.3:n.1084-492_1084-491insCTCCCCTTCCTCTTTTGCACTGATTTT...
NR_120639.1:n.998-492_998-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
NR_120640.1:n.1751-492_1751-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
XM_006713702.1:c.757-492_757-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT XP_006713765.1:n.757-492_757-491insCTCCCCTTCCTCTTTTGCACTGATTT...
XM_011512992.1:c.970-492_970-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT XP_011511294.1:n.970-492_970-491insCTCCCCTTCCTCTTTTGCACTGATTT...
XM_011512993.1:c.1084-492_1084-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT XP_011511295.1:n.1084-492_1084-491insCTCCCCTTCCTCTTTTGCACTGAT...
XR_241502.2:n.1231-492_1231-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
XR_924159.1:n.1231-492_1231-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
NM_001363880.1:c.757-492_757-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT NP_001350809.1:n.757-492_757-491insCTCCCCTTCCTCTTTTGCACTGATTT...
XM_011512992.2:c.970-492_970-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT XP_011511294.1:n.970-492_970-491insCTCCCCTTCCTCTTTTGCACTGATTT...
XR_001740207.2:n.1207-492_1207-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
XR_001740208.2:n.1207-492_1207-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
XR_001740209.2:n.1177-492_1177-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
XR_001740210.1:n.1037-492_1037-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
XR_002959553.1:n.1207-492_1207-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
XR_002959554.1:n.1207-492_1207-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
XR_241502.3:n.1177-492_1177-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
NM_020166.5:c.1084-492_1084-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT MANE Select NP_064551.3:n.1084-492_1084-491insCTCCCCTTCCTCTTTTGCACTGATTTT...
NM_001293273.2:c.733-492_733-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT NP_001280202.1:n.733-492_733-491insCTCCCCTTCCTCTTTTGCACTGATTT...
NR_120639.2:n.907-492_907-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT
NR_120640.2:n.1751-492_1751-491insCTCCCCTTCCTCTTTTGCACTGATTTTCAGCTTTTGCTTTTT