Canonical Allele Identifier: CA437092425

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182755076T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037288T>C , CM000665.2:g.183037288T>C	GRCh38
NC_000003.11:g.182755076T>C , CM000665.1:g.182755076T>C	GRCh37
NC_000003.10:g.184237770T>C	NCBI36
NG_008100.1:g.67290A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1524A>G MANE Select	ENSP00000265594.4:p.Leu508=
ENST00000265594.8:c.1524A>G	ENSP00000265594.4:p.Leu508=
ENST00000476176.5:c.1383A>G	ENSP00000420433.1:p.Leu461=
ENST00000489909.1:n.68A>G
ENST00000492597.5:c.1197A>G	ENSP00000419898.1:p.Leu399=
ENST00000495767.5:c.*1105A>G	ENSP00000419658.1:n.*1105A>G
ENST00000497830.5:c.*1121A>G	ENSP00000420088.1:n.*1121A>G
ENST00000497959.5:c.1263+1738A>G	ENSP00000420648.1:n.1263+1738A>G
ENST00000539926.5:c.1074A>G	ENSP00000441253.2:p.Leu358=
ENST00000610757.4:c.1074A>G	ENSP00000480435.1:p.Leu358=
ENST00000629669.2:c.1263+1738A>G	ENSP00000486824.1:n.1263+1738A>G
NM_001293273.1:c.1173A>G	NP_001280202.1:p.Leu391=
NM_020166.4:c.1524A>G	NP_064551.3:p.Leu508=
NR_120639.1:n.1438A>G
NR_120640.1:n.2044+1738A>G
XM_006713702.1:c.1197A>G	XP_006713765.1:p.Leu399=
XM_011512992.1:c.1410A>G	XP_011511294.1:p.Leu470=
XM_011512993.1:c.1377+1738A>G	XP_011511295.1:n.1377+1738A>G
XR_241502.2:n.1524+1738A>G
XR_924159.1:n.1671A>G
NM_001363880.1:c.1197A>G	NP_001350809.1:p.Leu399=
XM_011512992.2:c.1410A>G	XP_011511294.1:p.Leu470=
XR_001740207.2:n.1647A>G
XR_001740208.2:n.1647A>G
XR_001740209.2:n.1470+1738A>G
XR_001740210.1:n.1477A>G
XR_002959553.1:n.1647A>G
XR_002959554.1:n.1500+1738A>G
XR_241502.3:n.1470+1738A>G
NM_020166.5:c.1524A>G MANE Select	NP_064551.3:p.Leu508=
NM_001293273.2:c.1173A>G	NP_001280202.1:p.Leu391=
NR_120639.2:n.1347A>G
NR_120640.2:n.2044+1738A>G