Canonical Allele Identifier: CA548366154

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183052252dup , CM000665.2:g.183052252dup	GRCh38
NC_000003.11:g.182770040dup , CM000665.1:g.182770040dup	GRCh37
NC_000003.10:g.184252734dup	NCBI36
NG_008100.1:g.52332dup

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.874-6dup MANE Select	NP_064551.3:n.874-6dup
ENST00000265594.9:c.874-6dup MANE Select	ENSP00000265594.4:n.874-6dup
NM_001293273.1:c.523-6dup	NP_001280202.1:n.523-6dup
NM_001293273.2:c.523-6dup	NP_001280202.1:n.523-6dup
NM_001363880.1:c.547-6dup	NP_001350809.1:n.547-6dup
NM_020166.4:c.874-6dup	NP_064551.3:n.874-6dup
NR_120639.1:n.788-6dup
NR_120639.2:n.697-6dup
NR_120640.1:n.1541-6dup
NR_120640.2:n.1541-6dup
ENST00000265594.8:c.874-6dup	ENSP00000265594.4:n.874-6dup
ENST00000476176.5:c.733-6dup	ENSP00000420433.1:n.733-6dup
ENST00000492597.5:c.547-6dup	ENSP00000419898.1:n.547-6dup
ENST00000495767.5:c.*455-6dup	ENSP00000419658.1:n.*455-6dup
ENST00000497830.5:c.*471-6dup	ENSP00000420088.1:n.*471-6dup
ENST00000497959.5:c.760-6dup	ENSP00000420648.1:n.760-6dup
ENST00000539926.5:c.424-6dup	ENSP00000441253.2:n.424-6dup
ENST00000610757.4:c.424-6dup	ENSP00000480435.1:n.424-6dup
ENST00000629669.2:c.760-6dup	ENSP00000486824.1:n.760-6dup
XM_006713702.1:c.547-6dup	XP_006713765.1:n.547-6dup
XM_011512992.1:c.760-6dup	XP_011511294.1:n.760-6dup
XM_011512992.2:c.760-6dup	XP_011511294.1:n.760-6dup
XM_011512993.1:c.874-6dup	XP_011511295.1:n.874-6dup
XR_001740207.2:n.997-6dup
XR_001740208.2:n.997-6dup
XR_001740209.2:n.967-6dup
XR_001740210.1:n.827-6dup
XR_002959553.1:n.997-6dup
XR_002959554.1:n.997-6dup
XR_241502.2:n.1021-6dup
XR_241502.3:n.967-6dup
XR_924159.1:n.1021-6dup