Canonical Allele Identifier: CA437092429

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182755079A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037291A>G , CM000665.2:g.183037291A>G	GRCh38
NC_000003.11:g.182755079A>G , CM000665.1:g.182755079A>G	GRCh37
NC_000003.10:g.184237773A>G	NCBI36
NG_008100.1:g.67287T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1521T>C MANE Select	ENSP00000265594.4:p.Ser507=
ENST00000265594.8:c.1521T>C	ENSP00000265594.4:p.Ser507=
ENST00000476176.5:c.1380T>C	ENSP00000420433.1:p.Ser460=
ENST00000489909.1:n.65T>C
ENST00000492597.5:c.1194T>C	ENSP00000419898.1:p.Ser398=
ENST00000495767.5:c.*1102T>C	ENSP00000419658.1:n.*1102T>C
ENST00000497830.5:c.*1118T>C	ENSP00000420088.1:n.*1118T>C
ENST00000497959.5:c.1263+1735T>C	ENSP00000420648.1:n.1263+1735T>C
ENST00000539926.5:c.1071T>C	ENSP00000441253.2:p.Ser357=
ENST00000610757.4:c.1071T>C	ENSP00000480435.1:p.Ser357=
ENST00000629669.2:c.1263+1735T>C	ENSP00000486824.1:n.1263+1735T>C
NM_001293273.1:c.1170T>C	NP_001280202.1:p.Ser390=
NM_020166.4:c.1521T>C	NP_064551.3:p.Ser507=
NR_120639.1:n.1435T>C
NR_120640.1:n.2044+1735T>C
XM_006713702.1:c.1194T>C	XP_006713765.1:p.Ser398=
XM_011512992.1:c.1407T>C	XP_011511294.1:p.Ser469=
XM_011512993.1:c.1377+1735T>C	XP_011511295.1:n.1377+1735T>C
XR_241502.2:n.1524+1735T>C
XR_924159.1:n.1668T>C
NM_001363880.1:c.1194T>C	NP_001350809.1:p.Ser398=
XM_011512992.2:c.1407T>C	XP_011511294.1:p.Ser469=
XR_001740207.2:n.1644T>C
XR_001740208.2:n.1644T>C
XR_001740209.2:n.1470+1735T>C
XR_001740210.1:n.1474T>C
XR_002959553.1:n.1644T>C
XR_002959554.1:n.1500+1735T>C
XR_241502.3:n.1470+1735T>C
NM_020166.5:c.1521T>C MANE Select	NP_064551.3:p.Ser507=
NM_001293273.2:c.1170T>C	NP_001280202.1:p.Ser390=
NR_120639.2:n.1344T>C
NR_120640.2:n.2044+1735T>C