Canonical Allele Identifier: CA437092760

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182756832G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039044G>A , CM000665.2:g.183039044G>A	GRCh38
NC_000003.11:g.182756832G>A , CM000665.1:g.182756832G>A	GRCh37
NC_000003.10:g.184239526G>A	NCBI36
NG_008100.1:g.65534C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1359C>T MANE Select	ENSP00000265594.4:p.Tyr453=
ENST00000265594.8:c.1359C>T	ENSP00000265594.4:p.Tyr453=
ENST00000476176.5:c.1218C>T	ENSP00000420433.1:p.Tyr406=
ENST00000492597.5:c.1032C>T	ENSP00000419898.1:p.Tyr344=
ENST00000495767.5:c.*940C>T	ENSP00000419658.1:n.*940C>T
ENST00000497830.5:c.*956C>T	ENSP00000420088.1:n.*956C>T
ENST00000497959.5:c.1245C>T	ENSP00000420648.1:p.Tyr415=
ENST00000539926.5:c.909C>T	ENSP00000441253.2:p.Tyr303=
ENST00000610757.4:c.909C>T	ENSP00000480435.1:p.Tyr303=
ENST00000629669.2:c.1245C>T	ENSP00000486824.1:p.Tyr415=
NM_001293273.1:c.1008C>T	NP_001280202.1:p.Tyr336=
NM_020166.4:c.1359C>T	NP_064551.3:p.Tyr453=
NR_120639.1:n.1273C>T
NR_120640.1:n.2026C>T
XM_006713702.1:c.1032C>T	XP_006713765.1:p.Tyr344=
XM_011512992.1:c.1245C>T	XP_011511294.1:p.Tyr415=
XM_011512993.1:c.1359C>T	XP_011511295.1:p.Tyr453=
XR_241502.2:n.1506C>T
XR_924159.1:n.1506C>T
NM_001363880.1:c.1032C>T	NP_001350809.1:p.Tyr344=
XM_011512992.2:c.1245C>T	XP_011511294.1:p.Tyr415=
XR_001740207.2:n.1482C>T
XR_001740208.2:n.1482C>T
XR_001740209.2:n.1452C>T
XR_001740210.1:n.1312C>T
XR_002959553.1:n.1482C>T
XR_002959554.1:n.1482C>T
XR_241502.3:n.1452C>T
NM_020166.5:c.1359C>T MANE Select	NP_064551.3:p.Tyr453=
NM_001293273.2:c.1008C>T	NP_001280202.1:p.Tyr336=
NR_120639.2:n.1182C>T
NR_120640.2:n.2026C>T