Canonical Allele Identifier: CA1425382877

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183038884_183038885delinsTC , CM000665.2:g.183038884_183038885delinsTC	GRCh38
NC_000003.11:g.182756672_182756673delinsTC , CM000665.1:g.182756672_182756673delinsTC	GRCh37
NC_000003.10:g.184239366_184239367delinsTC	NCBI36
NG_008100.1:g.65693_65694delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1377+141_1377+142delinsGA MANE Select	ENSP00000265594.4:n.1377+141_1377+142delinsGA
ENST00000265594.8:c.1377+141_1377+142delinsGA	ENSP00000265594.4:n.1377+141_1377+142delinsGA
ENST00000476176.5:c.1236+141_1236+142delinsGA	ENSP00000420433.1:n.1236+141_1236+142delinsGA
ENST00000492597.5:c.1050+141_1050+142delinsGA	ENSP00000419898.1:n.1050+141_1050+142delinsGA
ENST00000495767.5:c.*958+141_*958+142delinsGA	ENSP00000419658.1:n.*958+141_*958+142delinsGA
ENST00000497830.5:c.*974+141_*974+142delinsGA	ENSP00000420088.1:n.*974+141_*974+142delinsGA
ENST00000497959.5:c.1263+141_1263+142delinsGA	ENSP00000420648.1:n.1263+141_1263+142delinsGA
ENST00000539926.5:c.927+141_927+142delinsGA	ENSP00000441253.2:n.927+141_927+142delinsGA
ENST00000610757.4:c.927+141_927+142delinsGA	ENSP00000480435.1:n.927+141_927+142delinsGA
ENST00000629669.2:c.1263+141_1263+142delinsGA	ENSP00000486824.1:n.1263+141_1263+142delinsGA
NM_001293273.1:c.1026+141_1026+142delinsGA	NP_001280202.1:n.1026+141_1026+142delinsGA
NM_020166.4:c.1377+141_1377+142delinsGA	NP_064551.3:n.1377+141_1377+142delinsGA
NR_120639.1:n.1291+141_1291+142delinsGA
NR_120640.1:n.2044+141_2044+142delinsGA
XM_006713702.1:c.1050+141_1050+142delinsGA	XP_006713765.1:n.1050+141_1050+142delinsGA
XM_011512992.1:c.1263+141_1263+142delinsGA	XP_011511294.1:n.1263+141_1263+142delinsGA
XM_011512993.1:c.1377+141_1377+142delinsGA	XP_011511295.1:n.1377+141_1377+142delinsGA
XR_241502.2:n.1524+141_1524+142delinsGA
XR_924159.1:n.1524+141_1524+142delinsGA
NM_001363880.1:c.1050+141_1050+142delinsGA	NP_001350809.1:n.1050+141_1050+142delinsGA
XM_011512992.2:c.1263+141_1263+142delinsGA	XP_011511294.1:n.1263+141_1263+142delinsGA
XR_001740207.2:n.1500+141_1500+142delinsGA
XR_001740208.2:n.1500+141_1500+142delinsGA
XR_001740209.2:n.1470+141_1470+142delinsGA
XR_001740210.1:n.1330+141_1330+142delinsGA
XR_002959553.1:n.1500+141_1500+142delinsGA
XR_002959554.1:n.1500+141_1500+142delinsGA
XR_241502.3:n.1470+141_1470+142delinsGA
NM_020166.5:c.1377+141_1377+142delinsGA MANE Select	NP_064551.3:n.1377+141_1377+142delinsGA
NM_001293273.2:c.1026+141_1026+142delinsGA	NP_001280202.1:n.1026+141_1026+142delinsGA
NR_120639.2:n.1200+141_1200+142delinsGA
NR_120640.2:n.2044+141_2044+142delinsGA