Canonical Allele Identifier: CA437092846

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182756895G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039107G>T , CM000665.2:g.183039107G>T	GRCh38
NC_000003.11:g.182756895G>T , CM000665.1:g.182756895G>T	GRCh37
NC_000003.10:g.184239589G>T	NCBI36
NG_008100.1:g.65471C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1296C>A MANE Select	ENSP00000265594.4:p.Pro432=
ENST00000265594.8:c.1296C>A	ENSP00000265594.4:p.Pro432=
ENST00000476176.5:c.1155C>A	ENSP00000420433.1:p.Pro385=
ENST00000492597.5:c.969C>A	ENSP00000419898.1:p.Pro323=
ENST00000495767.5:c.*877C>A	ENSP00000419658.1:n.*877C>A
ENST00000497830.5:c.*893C>A	ENSP00000420088.1:n.*893C>A
ENST00000497959.5:c.1182C>A	ENSP00000420648.1:p.Pro394=
ENST00000539926.5:c.846C>A	ENSP00000441253.2:p.Pro282=
ENST00000610757.4:c.846C>A	ENSP00000480435.1:p.Pro282=
ENST00000629669.2:c.1182C>A	ENSP00000486824.1:p.Pro394=
NM_001293273.1:c.945C>A	NP_001280202.1:p.Pro315=
NM_020166.4:c.1296C>A	NP_064551.3:p.Pro432=
NR_120639.1:n.1210C>A
NR_120640.1:n.1963C>A
XM_006713702.1:c.969C>A	XP_006713765.1:p.Pro323=
XM_011512992.1:c.1182C>A	XP_011511294.1:p.Pro394=
XM_011512993.1:c.1296C>A	XP_011511295.1:p.Pro432=
XR_241502.2:n.1443C>A
XR_924159.1:n.1443C>A
NM_001363880.1:c.969C>A	NP_001350809.1:p.Pro323=
XM_011512992.2:c.1182C>A	XP_011511294.1:p.Pro394=
XR_001740207.2:n.1419C>A
XR_001740208.2:n.1419C>A
XR_001740209.2:n.1389C>A
XR_001740210.1:n.1249C>A
XR_002959553.1:n.1419C>A
XR_002959554.1:n.1419C>A
XR_241502.3:n.1389C>A
NM_020166.5:c.1296C>A MANE Select	NP_064551.3:p.Pro432=
NM_001293273.2:c.945C>A	NP_001280202.1:p.Pro315=
NR_120639.2:n.1119C>A
NR_120640.2:n.1963C>A