Canonical Allele Identifier: CA1425382937

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039015_183039016delinsAG , CM000665.2:g.183039015_183039016delinsAG	GRCh38
NC_000003.11:g.182756803_182756804delinsAG , CM000665.1:g.182756803_182756804delinsAG	GRCh37
NC_000003.10:g.184239497_184239498delinsAG	NCBI36
NG_008100.1:g.65562_65563delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000265594.9:c.1377+10_1377+11delinsCT MANE Select	ENSP00000265594.4:n.1377+10_1377+11delins...
ENST00000265594.8:c.1377+10_1377+11delinsCT	ENSP00000265594.4:n.1377+10_1377+11delins...
ENST00000476176.5:c.1236+10_1236+11delinsCT	ENSP00000420433.1:n.1236+10_1236+11delins...
ENST00000492597.5:c.1050+10_1050+11delinsCT	ENSP00000419898.1:n.1050+10_1050+11delins...
ENST00000495767.5:c.*958+10_*958+11delinsCT	ENSP00000419658.1:n.*958+10_*958+11delins...
ENST00000497830.5:c.*974+10_*974+11delinsCT	ENSP00000420088.1:n.*974+10_*974+11delins...
ENST00000497959.5:c.1263+10_1263+11delinsCT	ENSP00000420648.1:n.1263+10_1263+11delins...
ENST00000539926.5:c.927+10_927+11delinsCT	ENSP00000441253.2:n.927+10_927+11delinsCT...
ENST00000610757.4:c.927+10_927+11delinsCT	ENSP00000480435.1:n.927+10_927+11delinsCT...
ENST00000629669.2:c.1263+10_1263+11delinsCT	ENSP00000486824.1:n.1263+10_1263+11delins...
NM_001293273.1:c.1026+10_1026+11delinsCT	NP_001280202.1:n.1026+10_1026+11delinsCT
NM_020166.4:c.1377+10_1377+11delinsCT	NP_064551.3:n.1377+10_1377+11delinsCT
NR_120639.1:n.1291+10_1291+11delinsCT
NR_120640.1:n.2044+10_2044+11delinsCT
XM_006713702.1:c.1050+10_1050+11delinsCT	XP_006713765.1:n.1050+10_1050+11delinsCT
XM_011512992.1:c.1263+10_1263+11delinsCT	XP_011511294.1:n.1263+10_1263+11delinsCT
XM_011512993.1:c.1377+10_1377+11delinsCT	XP_011511295.1:n.1377+10_1377+11delinsCT
XR_241502.2:n.1524+10_1524+11delinsCT
XR_924159.1:n.1524+10_1524+11delinsCT
NM_001363880.1:c.1050+10_1050+11delinsCT	NP_001350809.1:n.1050+10_1050+11delinsCT
XM_011512992.2:c.1263+10_1263+11delinsCT	XP_011511294.1:n.1263+10_1263+11delinsCT
XR_001740207.2:n.1500+10_1500+11delinsCT
XR_001740208.2:n.1500+10_1500+11delinsCT
XR_001740209.2:n.1470+10_1470+11delinsCT
XR_001740210.1:n.1330+10_1330+11delinsCT
XR_002959553.1:n.1500+10_1500+11delinsCT
XR_002959554.1:n.1500+10_1500+11delinsCT
XR_241502.3:n.1470+10_1470+11delinsCT
NM_020166.5:c.1377+10_1377+11delinsCT MANE Select	NP_064551.3:n.1377+10_1377+11delinsCT
NM_001293273.2:c.1026+10_1026+11delinsCT	NP_001280202.1:n.1026+10_1026+11delinsCT
NR_120639.2:n.1200+10_1200+11delinsCT
NR_120640.2:n.2044+10_2044+11delinsCT