Canonical Allele Identifier: CA88702185

Gene: MCCC1

Linked Data

• ClinVar Variation Id: 3124197
• ClinVar RCV Id: RCV004419073
• dbSNP Id: rs369093010
• gnomAD v2: 3-182756918-C-G
• gnomAD v3: 3-183039130-C-G
• gnomAD v4: 3-183039130-C-G
• MyVariant Identifiers: chr3:g.182756918C>G (hg19) ; chr3:g.183039130C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039130C>G , CM000665.2:g.183039130C>G	GRCh38
NC_000003.11:g.182756918C>G , CM000665.1:g.182756918C>G	GRCh37
NC_000003.10:g.184239612C>G	NCBI36
NG_008100.1:g.65448G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1273G>C MANE Select	ENSP00000265594.4:p.Glu425Gln
ENST00000265594.8:c.1273G>C	ENSP00000265594.4:p.Glu425Gln
ENST00000476176.5:c.1132G>C	ENSP00000420433.1:p.Glu378Gln
ENST00000492597.5:c.946G>C	ENSP00000419898.1:p.Glu316Gln
ENST00000495767.5:c.*854G>C	ENSP00000419658.1:n.*854G>C
ENST00000497830.5:c.*870G>C	ENSP00000420088.1:n.*870G>C
ENST00000497959.5:c.1159G>C	ENSP00000420648.1:p.Glu387Gln
ENST00000539926.5:c.823G>C	ENSP00000441253.2:p.Glu275Gln
ENST00000610757.4:c.823G>C	ENSP00000480435.1:p.Glu275Gln
ENST00000629669.2:c.1159G>C	ENSP00000486824.1:p.Glu387Gln
NM_001293273.1:c.922G>C	NP_001280202.1:p.Glu308Gln
NM_020166.4:c.1273G>C	NP_064551.3:p.Glu425Gln
NR_120639.1:n.1187G>C
NR_120640.1:n.1940G>C
XM_006713702.1:c.946G>C	XP_006713765.1:p.Glu316Gln
XM_011512992.1:c.1159G>C	XP_011511294.1:p.Glu387Gln
XM_011512993.1:c.1273G>C	XP_011511295.1:p.Glu425Gln
XR_241502.2:n.1420G>C
XR_924159.1:n.1420G>C
NM_001363880.1:c.946G>C	NP_001350809.1:p.Glu316Gln
XM_011512992.2:c.1159G>C	XP_011511294.1:p.Glu387Gln
XR_001740207.2:n.1396G>C
XR_001740208.2:n.1396G>C
XR_001740209.2:n.1366G>C
XR_001740210.1:n.1226G>C
XR_002959553.1:n.1396G>C
XR_002959554.1:n.1396G>C
XR_241502.3:n.1366G>C
NM_020166.5:c.1273G>C MANE Select	NP_064551.3:p.Glu425Gln
NM_001293273.2:c.922G>C	NP_001280202.1:p.Glu308Gln
NR_120639.2:n.1096G>C
NR_120640.2:n.1940G>C