Canonical Allele Identifier: CA437092585

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182755217A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037429A>G , CM000665.2:g.183037429A>G	GRCh38
NC_000003.11:g.182755217A>G , CM000665.1:g.182755217A>G	GRCh37
NC_000003.10:g.184237911A>G	NCBI36
NG_008100.1:g.67149T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1383T>C MANE Select	ENSP00000265594.4:p.Val461=
ENST00000265594.8:c.1383T>C	ENSP00000265594.4:p.Val461=
ENST00000476176.5:c.1242T>C	ENSP00000420433.1:p.Val414=
ENST00000492597.5:c.1056T>C	ENSP00000419898.1:p.Val352=
ENST00000495767.5:c.*964T>C	ENSP00000419658.1:n.*964T>C
ENST00000497830.5:c.*980T>C	ENSP00000420088.1:n.*980T>C
ENST00000497959.5:c.1263+1597T>C	ENSP00000420648.1:n.1263+1597T>C
ENST00000539926.5:c.933T>C	ENSP00000441253.2:p.Val311=
ENST00000610757.4:c.933T>C	ENSP00000480435.1:p.Val311=
ENST00000629669.2:c.1263+1597T>C	ENSP00000486824.1:n.1263+1597T>C
NM_001293273.1:c.1032T>C	NP_001280202.1:p.Val344=
NM_020166.4:c.1383T>C	NP_064551.3:p.Val461=
NR_120639.1:n.1297T>C
NR_120640.1:n.2044+1597T>C
XM_006713702.1:c.1056T>C	XP_006713765.1:p.Val352=
XM_011512992.1:c.1269T>C	XP_011511294.1:p.Val423=
XM_011512993.1:c.1377+1597T>C	XP_011511295.1:n.1377+1597T>C
XR_241502.2:n.1524+1597T>C
XR_924159.1:n.1530T>C
NM_001363880.1:c.1056T>C	NP_001350809.1:p.Val352=
XM_011512992.2:c.1269T>C	XP_011511294.1:p.Val423=
XR_001740207.2:n.1506T>C
XR_001740208.2:n.1506T>C
XR_001740209.2:n.1470+1597T>C
XR_001740210.1:n.1336T>C
XR_002959553.1:n.1506T>C
XR_002959554.1:n.1500+1597T>C
XR_241502.3:n.1470+1597T>C
NM_020166.5:c.1383T>C MANE Select	NP_064551.3:p.Val461=
NM_001293273.2:c.1032T>C	NP_001280202.1:p.Val344=
NR_120639.2:n.1206T>C
NR_120640.2:n.2044+1597T>C