Canonical Allele Identifier: CA355319841

Gene: MCCC1

Linked Data

• ClinVar Variation Id: 2676447
• ClinVar RCV Id: RCV003470056
• MyVariant Identifiers: chr3:g.182755015G>A (hg19) ; chr3:g.183037227G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037227G>A , CM000665.2:g.183037227G>A	GRCh38
NC_000003.11:g.182755015G>A , CM000665.1:g.182755015G>A	GRCh37
NC_000003.10:g.184237709G>A	NCBI36
NG_008100.1:g.67351C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1585C>T MANE Select	ENSP00000265594.4:p.Gln529Ter
ENST00000265594.8:c.1585C>T	ENSP00000265594.4:p.Gln529Ter
ENST00000476176.5:c.1444C>T	ENSP00000420433.1:p.Gln482Ter
ENST00000489909.1:n.129C>T
ENST00000492597.5:c.1258C>T	ENSP00000419898.1:p.Gln420Ter
ENST00000495767.5:c.*1166C>T	ENSP00000419658.1:n.*1166C>T
ENST00000497830.5:c.*1182C>T	ENSP00000420088.1:n.*1182C>T
ENST00000497959.5:c.1263+1799C>T	ENSP00000420648.1:n.1263+1799C>T
ENST00000539926.5:c.1135C>T	ENSP00000441253.2:p.Gln379Ter
ENST00000610757.4:c.1135C>T	ENSP00000480435.1:p.Gln379Ter
ENST00000629669.2:c.1263+1799C>T	ENSP00000486824.1:n.1263+1799C>T
NM_001293273.1:c.1234C>T	NP_001280202.1:p.Gln412Ter
NM_020166.4:c.1585C>T	NP_064551.3:p.Gln529Ter
NR_120639.1:n.1499C>T
NR_120640.1:n.2044+1799C>T
XM_006713702.1:c.1258C>T	XP_006713765.1:p.Gln420Ter
XM_011512992.1:c.1471C>T	XP_011511294.1:p.Gln491Ter
XM_011512993.1:c.1377+1799C>T	XP_011511295.1:n.1377+1799C>T
XR_241502.2:n.1524+1799C>T
XR_924159.1:n.1732C>T
NM_001363880.1:c.1258C>T	NP_001350809.1:p.Gln420Ter
XM_011512992.2:c.1471C>T	XP_011511294.1:p.Gln491Ter
XR_001740207.2:n.1708C>T
XR_001740208.2:n.1708C>T
XR_001740209.2:n.1470+1799C>T
XR_001740210.1:n.1538C>T
XR_002959553.1:n.1708C>T
XR_002959554.1:n.1500+1799C>T
XR_241502.3:n.1470+1799C>T
NM_020166.5:c.1585C>T MANE Select	NP_064551.3:p.Gln529Ter
NM_001293273.2:c.1234C>T	NP_001280202.1:p.Gln412Ter
NR_120639.2:n.1408C>T
NR_120640.2:n.2044+1799C>T