Canonical Allele Identifier: CA1425383073

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039333_183039334delinsAC , CM000665.2:g.183039333_183039334delinsAC	GRCh38
NC_000003.11:g.182757121_182757122delinsAC , CM000665.1:g.182757121_182757122delinsAC	GRCh37
NC_000003.10:g.184239815_184239816delinsAC	NCBI36
NG_008100.1:g.65244_65245delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1268-199_1268-198delinsGT MANE Select	ENSP00000265594.4:n.1268-199_1268-198delinsGT
ENST00000265594.8:c.1268-199_1268-198delinsGT	ENSP00000265594.4:n.1268-199_1268-198delinsGT
ENST00000476176.5:c.1127-199_1127-198delinsGT	ENSP00000420433.1:n.1127-199_1127-198delinsGT
ENST00000492597.5:c.941-199_941-198delinsGT	ENSP00000419898.1:n.941-199_941-198delinsGT
ENST00000495767.5:c.*849-199_*849-198delinsGT	ENSP00000419658.1:n.*849-199_*849-198delinsGT
ENST00000497830.5:c.*865-199_*865-198delinsGT	ENSP00000420088.1:n.*865-199_*865-198delinsGT
ENST00000497959.5:c.1154-199_1154-198delinsGT	ENSP00000420648.1:n.1154-199_1154-198delinsGT
ENST00000539926.5:c.818-199_818-198delinsGT	ENSP00000441253.2:n.818-199_818-198delinsGT
ENST00000610757.4:c.818-199_818-198delinsGT	ENSP00000480435.1:n.818-199_818-198delinsGT
ENST00000629669.2:c.1154-199_1154-198delinsGT	ENSP00000486824.1:n.1154-199_1154-198delinsGT
NM_001293273.1:c.917-199_917-198delinsGT	NP_001280202.1:n.917-199_917-198delinsGT
NM_020166.4:c.1268-199_1268-198delinsGT	NP_064551.3:n.1268-199_1268-198delinsGT
NR_120639.1:n.1182-199_1182-198delinsGT
NR_120640.1:n.1935-199_1935-198delinsGT
XM_006713702.1:c.941-199_941-198delinsGT	XP_006713765.1:n.941-199_941-198delinsGT
XM_011512992.1:c.1154-199_1154-198delinsGT	XP_011511294.1:n.1154-199_1154-198delinsGT
XM_011512993.1:c.1268-199_1268-198delinsGT	XP_011511295.1:n.1268-199_1268-198delinsGT
XR_241502.2:n.1415-199_1415-198delinsGT
XR_924159.1:n.1415-199_1415-198delinsGT
NM_001363880.1:c.941-199_941-198delinsGT	NP_001350809.1:n.941-199_941-198delinsGT
XM_011512992.2:c.1154-199_1154-198delinsGT	XP_011511294.1:n.1154-199_1154-198delinsGT
XR_001740207.2:n.1391-199_1391-198delinsGT
XR_001740208.2:n.1391-199_1391-198delinsGT
XR_001740209.2:n.1361-199_1361-198delinsGT
XR_001740210.1:n.1221-199_1221-198delinsGT
XR_002959553.1:n.1391-199_1391-198delinsGT
XR_002959554.1:n.1391-199_1391-198delinsGT
XR_241502.3:n.1361-199_1361-198delinsGT
NM_020166.5:c.1268-199_1268-198delinsGT MANE Select	NP_064551.3:n.1268-199_1268-198delinsGT
NM_001293273.2:c.917-199_917-198delinsGT	NP_001280202.1:n.917-199_917-198delinsGT
NR_120639.2:n.1091-199_1091-198delinsGT
NR_120640.2:n.1935-199_1935-198delinsGT