Canonical Allele Identifier: CA2718892

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183045422C>T , CM000665.2:g.183045422C>T	GRCh38
NC_000003.11:g.182763210C>T , CM000665.1:g.182763210C>T	GRCh37
NC_000003.10:g.184245904C>T	NCBI36
NG_008100.1:g.59156G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.1074G>A MANE Select	NP_064551.3:p.Trp358Ter
ENST00000265594.9:c.1074G>A MANE Select	ENSP00000265594.4:p.Trp358Ter
NM_001293273.1:c.723G>A	NP_001280202.1:p.Trp241Ter
NM_001293273.2:c.723G>A	NP_001280202.1:p.Trp241Ter
NM_001363880.1:c.747G>A	NP_001350809.1:p.Trp249Ter
NM_020166.4:c.1074G>A	NP_064551.3:p.Trp358Ter
NR_120639.1:n.988G>A
NR_120639.2:n.897G>A
NR_120640.1:n.1741G>A
NR_120640.2:n.1741G>A
ENST00000265594.8:c.1074G>A	ENSP00000265594.4:p.Trp358Ter
ENST00000476176.5:c.933G>A	ENSP00000420433.1:p.Trp311Ter
ENST00000492597.5:c.747G>A	ENSP00000419898.1:p.Trp249Ter
ENST00000495767.5:c.*655G>A	ENSP00000419658.1:n.*655G>A
ENST00000497830.5:c.*671G>A	ENSP00000420088.1:n.*671G>A
ENST00000497959.5:c.960G>A	ENSP00000420648.1:p.Trp320Ter
ENST00000539926.5:c.624G>A	ENSP00000441253.2:p.Trp208Ter
ENST00000610757.4:c.624G>A	ENSP00000480435.1:p.Trp208Ter
ENST00000629669.2:c.960G>A	ENSP00000486824.1:p.Trp320Ter
XM_006713702.1:c.747G>A	XP_006713765.1:p.Trp249Ter
XM_011512992.1:c.960G>A	XP_011511294.1:p.Trp320Ter
XM_011512992.2:c.960G>A	XP_011511294.1:p.Trp320Ter
XM_011512993.1:c.1074G>A	XP_011511295.1:p.Trp358Ter
XR_001740207.2:n.1197G>A
XR_001740208.2:n.1197G>A
XR_001740209.2:n.1167G>A
XR_001740210.1:n.1027G>A
XR_002959553.1:n.1197G>A
XR_002959554.1:n.1197G>A
XR_241502.2:n.1221G>A
XR_241502.3:n.1167G>A
XR_924159.1:n.1221G>A