Canonical Allele Identifier: CA274959

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183041720G>A , CM000665.2:g.183041720G>A	GRCh38
NC_000003.11:g.182759508G>A , CM000665.1:g.182759508G>A	GRCh37
NC_000003.10:g.184242202G>A	NCBI36
NG_008100.1:g.62858C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.1114C>T MANE Select	NP_064551.3:p.Gln372Ter
ENST00000265594.9:c.1114C>T MANE Select	ENSP00000265594.4:p.Gln372Ter
NM_001293273.1:c.763C>T	NP_001280202.1:p.Gln255Ter
NM_001293273.2:c.763C>T	NP_001280202.1:p.Gln255Ter
NM_001363880.1:c.787C>T	NP_001350809.1:p.Gln263Ter
NM_020166.4:c.1114C>T	NP_064551.3:p.Gln372Ter
NR_120639.1:n.1028C>T
NR_120639.2:n.937C>T
NR_120640.1:n.1781C>T
NR_120640.2:n.1781C>T
ENST00000265594.8:c.1114C>T	ENSP00000265594.4:p.Gln372Ter
ENST00000476176.5:c.973C>T	ENSP00000420433.1:p.Gln325Ter
ENST00000492597.5:c.787C>T	ENSP00000419898.1:p.Gln263Ter
ENST00000495767.5:c.*695C>T	ENSP00000419658.1:n.*695C>T
ENST00000497830.5:c.*711C>T	ENSP00000420088.1:n.*711C>T
ENST00000497959.5:c.1000C>T	ENSP00000420648.1:p.Gln334Ter
ENST00000539926.5:c.664C>T	ENSP00000441253.2:p.Gln222Ter
ENST00000610757.4:c.664C>T	ENSP00000480435.1:p.Gln222Ter
ENST00000629669.2:c.1000C>T	ENSP00000486824.1:p.Gln334Ter
XM_006713702.1:c.787C>T	XP_006713765.1:p.Gln263Ter
XM_011512992.1:c.1000C>T	XP_011511294.1:p.Gln334Ter
XM_011512992.2:c.1000C>T	XP_011511294.1:p.Gln334Ter
XM_011512993.1:c.1114C>T	XP_011511295.1:p.Gln372Ter
XR_001740207.2:n.1237C>T
XR_001740208.2:n.1237C>T
XR_001740209.2:n.1207C>T
XR_001740210.1:n.1067C>T
XR_002959553.1:n.1237C>T
XR_002959554.1:n.1237C>T
XR_241502.2:n.1261C>T
XR_241502.3:n.1207C>T
XR_924159.1:n.1261C>T