Canonical Allele Identifier: CA355319974

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182755039C>G (hg19) ; chr3:g.183037251C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037251C>G , CM000665.2:g.183037251C>G	GRCh38
NC_000003.11:g.182755039C>G , CM000665.1:g.182755039C>G	GRCh37
NC_000003.10:g.184237733C>G	NCBI36
NG_008100.1:g.67327G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1561G>C MANE Select	ENSP00000265594.4:p.Ala521Pro
ENST00000265594.8:c.1561G>C	ENSP00000265594.4:p.Ala521Pro
ENST00000476176.5:c.1420G>C	ENSP00000420433.1:p.Ala474Pro
ENST00000489909.1:n.105G>C
ENST00000492597.5:c.1234G>C	ENSP00000419898.1:p.Ala412Pro
ENST00000495767.5:c.*1142G>C	ENSP00000419658.1:n.*1142G>C
ENST00000497830.5:c.*1158G>C	ENSP00000420088.1:n.*1158G>C
ENST00000497959.5:c.1263+1775G>C	ENSP00000420648.1:n.1263+1775G>C
ENST00000539926.5:c.1111G>C	ENSP00000441253.2:p.Ala371Pro
ENST00000610757.4:c.1111G>C	ENSP00000480435.1:p.Ala371Pro
ENST00000629669.2:c.1263+1775G>C	ENSP00000486824.1:n.1263+1775G>C
NM_001293273.1:c.1210G>C	NP_001280202.1:p.Ala404Pro
NM_020166.4:c.1561G>C	NP_064551.3:p.Ala521Pro
NR_120639.1:n.1475G>C
NR_120640.1:n.2044+1775G>C
XM_006713702.1:c.1234G>C	XP_006713765.1:p.Ala412Pro
XM_011512992.1:c.1447G>C	XP_011511294.1:p.Ala483Pro
XM_011512993.1:c.1377+1775G>C	XP_011511295.1:n.1377+1775G>C
XR_241502.2:n.1524+1775G>C
XR_924159.1:n.1708G>C
NM_001363880.1:c.1234G>C	NP_001350809.1:p.Ala412Pro
XM_011512992.2:c.1447G>C	XP_011511294.1:p.Ala483Pro
XR_001740207.2:n.1684G>C
XR_001740208.2:n.1684G>C
XR_001740209.2:n.1470+1775G>C
XR_001740210.1:n.1514G>C
XR_002959553.1:n.1684G>C
XR_002959554.1:n.1500+1775G>C
XR_241502.3:n.1470+1775G>C
NM_020166.5:c.1561G>C MANE Select	NP_064551.3:p.Ala521Pro
NM_001293273.2:c.1210G>C	NP_001280202.1:p.Ala404Pro
NR_120639.2:n.1384G>C
NR_120640.2:n.2044+1775G>C