Canonical Allele Identifier: CA1425382929
Gene: MCCC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.183038999_183039000delinsTC , CM000665.2:g.183038999_183039000delinsTC GRCh38
NC_000003.11:g.182756787_182756788delinsTC , CM000665.1:g.182756787_182756788delinsTC GRCh37
NC_000003.10:g.184239481_184239482delinsTC NCBI36
NG_008100.1:g.65578_65579delinsGA

Transcript Alleles

HGVS Amino-acid change
ENST00000265594.9:c.1377+26_1377+27delinsGA MANE Select ENSP00000265594.4:n.1377+26_1377+27delins...
ENST00000265594.8:c.1377+26_1377+27delinsGA ENSP00000265594.4:n.1377+26_1377+27delins...
ENST00000476176.5:c.1236+26_1236+27delinsGA ENSP00000420433.1:n.1236+26_1236+27delins...
ENST00000492597.5:c.1050+26_1050+27delinsGA ENSP00000419898.1:n.1050+26_1050+27delins...
ENST00000495767.5:c.*958+26_*958+27delinsGA ENSP00000419658.1:n.*958+26_*958+27delins...
ENST00000497830.5:c.*974+26_*974+27delinsGA ENSP00000420088.1:n.*974+26_*974+27delins...
ENST00000497959.5:c.1263+26_1263+27delinsGA ENSP00000420648.1:n.1263+26_1263+27delins...
ENST00000539926.5:c.927+26_927+27delinsGA ENSP00000441253.2:n.927+26_927+27delinsGA...
ENST00000610757.4:c.927+26_927+27delinsGA ENSP00000480435.1:n.927+26_927+27delinsGA...
ENST00000629669.2:c.1263+26_1263+27delinsGA ENSP00000486824.1:n.1263+26_1263+27delins...
NM_001293273.1:c.1026+26_1026+27delinsGA NP_001280202.1:n.1026+26_1026+27delinsGA
NM_020166.4:c.1377+26_1377+27delinsGA NP_064551.3:n.1377+26_1377+27delinsGA
NR_120639.1:n.1291+26_1291+27delinsGA
NR_120640.1:n.2044+26_2044+27delinsGA
XM_006713702.1:c.1050+26_1050+27delinsGA XP_006713765.1:n.1050+26_1050+27delinsGA
XM_011512992.1:c.1263+26_1263+27delinsGA XP_011511294.1:n.1263+26_1263+27delinsGA
XM_011512993.1:c.1377+26_1377+27delinsGA XP_011511295.1:n.1377+26_1377+27delinsGA
XR_241502.2:n.1524+26_1524+27delinsGA
XR_924159.1:n.1524+26_1524+27delinsGA
NM_001363880.1:c.1050+26_1050+27delinsGA NP_001350809.1:n.1050+26_1050+27delinsGA
XM_011512992.2:c.1263+26_1263+27delinsGA XP_011511294.1:n.1263+26_1263+27delinsGA
XR_001740207.2:n.1500+26_1500+27delinsGA
XR_001740208.2:n.1500+26_1500+27delinsGA
XR_001740209.2:n.1470+26_1470+27delinsGA
XR_001740210.1:n.1330+26_1330+27delinsGA
XR_002959553.1:n.1500+26_1500+27delinsGA
XR_002959554.1:n.1500+26_1500+27delinsGA
XR_241502.3:n.1470+26_1470+27delinsGA
NM_020166.5:c.1377+26_1377+27delinsGA MANE Select NP_064551.3:n.1377+26_1377+27delinsGA
NM_001293273.2:c.1026+26_1026+27delinsGA NP_001280202.1:n.1026+26_1026+27delinsGA
NR_120639.2:n.1200+26_1200+27delinsGA
NR_120640.2:n.2044+26_2044+27delinsGA