Canonical Allele Identifier: CA355326458

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183052158C>T , CM000665.2:g.183052158C>T	GRCh38
NC_000003.11:g.182769946C>T , CM000665.1:g.182769946C>T	GRCh37
NC_000003.10:g.184252640C>T	NCBI36
NG_008100.1:g.52420G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.955+1G>A MANE Select	NP_064551.3:n.955+1G>A
ENST00000265594.9:c.955+1G>A MANE Select	ENSP00000265594.4:n.955+1G>A
NM_001293273.1:c.604+1G>A	NP_001280202.1:n.604+1G>A
NM_001293273.2:c.604+1G>A	NP_001280202.1:n.604+1G>A
NM_001363880.1:c.628+1G>A	NP_001350809.1:n.628+1G>A
NM_020166.4:c.955+1G>A	NP_064551.3:n.955+1G>A
NR_120639.1:n.869+1G>A
NR_120639.2:n.778+1G>A
NR_120640.1:n.1622+1G>A
NR_120640.2:n.1622+1G>A
ENST00000265594.8:c.955+1G>A	ENSP00000265594.4:n.955+1G>A
ENST00000476176.5:c.814+1G>A	ENSP00000420433.1:n.814+1G>A
ENST00000492597.5:c.628+1G>A	ENSP00000419898.1:n.628+1G>A
ENST00000495767.5:c.*536+1G>A	ENSP00000419658.1:n.*536+1G>A
ENST00000497830.5:c.*552+1G>A	ENSP00000420088.1:n.*552+1G>A
ENST00000497959.5:c.841+1G>A	ENSP00000420648.1:n.841+1G>A
ENST00000539926.5:c.505+1G>A	ENSP00000441253.2:n.505+1G>A
ENST00000610757.4:c.505+1G>A	ENSP00000480435.1:n.505+1G>A
ENST00000629669.2:c.841+1G>A	ENSP00000486824.1:n.841+1G>A
XM_006713702.1:c.628+1G>A	XP_006713765.1:n.628+1G>A
XM_011512992.1:c.841+1G>A	XP_011511294.1:n.841+1G>A
XM_011512992.2:c.841+1G>A	XP_011511294.1:n.841+1G>A
XM_011512993.1:c.955+1G>A	XP_011511295.1:n.955+1G>A
XR_001740207.2:n.1078+1G>A
XR_001740208.2:n.1078+1G>A
XR_001740209.2:n.1048+1G>A
XR_001740210.1:n.908+1G>A
XR_002959553.1:n.1078+1G>A
XR_002959554.1:n.1078+1G>A
XR_241502.2:n.1102+1G>A
XR_241502.3:n.1048+1G>A
XR_924159.1:n.1102+1G>A