Canonical Allele Identifier: CA355319863

Gene: MCCC1

Linked Data

• ClinVar Variation Id: 2200532
• ClinVar RCV Id: RCV002638263
• dbSNP Id: rs1446858208
• gnomAD v2: 3-182755020-G-A
• gnomAD v4: 3-183037232-G-A
• MyVariant Identifiers: chr3:g.182755020G>A (hg19) ; chr3:g.183037232G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037232G>A , CM000665.2:g.183037232G>A	GRCh38
NC_000003.11:g.182755020G>A , CM000665.1:g.182755020G>A	GRCh37
NC_000003.10:g.184237714G>A	NCBI36
NG_008100.1:g.67346C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1580C>T MANE Select	ENSP00000265594.4:p.Thr527Ile
ENST00000265594.8:c.1580C>T	ENSP00000265594.4:p.Thr527Ile
ENST00000476176.5:c.1439C>T	ENSP00000420433.1:p.Thr480Ile
ENST00000489909.1:n.124C>T
ENST00000492597.5:c.1253C>T	ENSP00000419898.1:p.Thr418Ile
ENST00000495767.5:c.*1161C>T	ENSP00000419658.1:n.*1161C>T
ENST00000497830.5:c.*1177C>T	ENSP00000420088.1:n.*1177C>T
ENST00000497959.5:c.1263+1794C>T	ENSP00000420648.1:n.1263+1794C>T
ENST00000539926.5:c.1130C>T	ENSP00000441253.2:p.Thr377Ile
ENST00000610757.4:c.1130C>T	ENSP00000480435.1:p.Thr377Ile
ENST00000629669.2:c.1263+1794C>T	ENSP00000486824.1:n.1263+1794C>T
NM_001293273.1:c.1229C>T	NP_001280202.1:p.Thr410Ile
NM_020166.4:c.1580C>T	NP_064551.3:p.Thr527Ile
NR_120639.1:n.1494C>T
NR_120640.1:n.2044+1794C>T
XM_006713702.1:c.1253C>T	XP_006713765.1:p.Thr418Ile
XM_011512992.1:c.1466C>T	XP_011511294.1:p.Thr489Ile
XM_011512993.1:c.1377+1794C>T	XP_011511295.1:n.1377+1794C>T
XR_241502.2:n.1524+1794C>T
XR_924159.1:n.1727C>T
NM_001363880.1:c.1253C>T	NP_001350809.1:p.Thr418Ile
XM_011512992.2:c.1466C>T	XP_011511294.1:p.Thr489Ile
XR_001740207.2:n.1703C>T
XR_001740208.2:n.1703C>T
XR_001740209.2:n.1470+1794C>T
XR_001740210.1:n.1533C>T
XR_002959553.1:n.1703C>T
XR_002959554.1:n.1500+1794C>T
XR_241502.3:n.1470+1794C>T
NM_020166.5:c.1580C>T MANE Select	NP_064551.3:p.Thr527Ile
NM_001293273.2:c.1229C>T	NP_001280202.1:p.Thr410Ile
NR_120639.2:n.1403C>T
NR_120640.2:n.2044+1794C>T