Canonical Allele Identifier: CA355319594

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183086774A>T , CM000665.2:g.183086774A>T	GRCh38
NC_000003.11:g.182804562A>T , CM000665.1:g.182804562A>T	GRCh37
NC_000003.10:g.184287256A>T	NCBI36
NG_008100.1:g.17804T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.288T>A MANE Select	NP_064551.3:p.Tyr96Ter
ENST00000265594.9:c.288T>A MANE Select	ENSP00000265594.4:p.Tyr96Ter
NM_001293273.1:c.59T>A	NP_001280202.1:p.Ile20Asn
NM_001293273.2:c.59T>A	NP_001280202.1:p.Ile20Asn
NM_001363880.1:c.-40T>A	NP_001350809.1:n.-40T>A
NM_020166.4:c.288T>A	NP_064551.3:p.Tyr96Ter
NR_120639.1:n.283+7785T>A
NR_120639.2:n.192+7785T>A
NR_120640.1:n.955T>A
NR_120640.2:n.955T>A
ENST00000265594.8:c.288T>A	ENSP00000265594.4:p.Tyr96Ter
ENST00000466650.5:c.*7T>A	ENSP00000418979.1:n.*7T>A
ENST00000476176.5:c.147T>A	ENSP00000420433.1:p.Tyr49Ter
ENST00000486226.1:c.*45T>A	ENSP00000420223.1:n.*45T>A
ENST00000487634.5:c.136+7785T>A	ENSP00000420591.1:n.136+7785T>A
ENST00000490284.5:c.89+12578T>A	ENSP00000419328.1:n.89+12578T>A
ENST00000492597.5:c.-40T>A	ENSP00000419898.1:n.-40T>A
ENST00000495767.5:c.136+7785T>A	ENSP00000419658.1:n.136+7785T>A
ENST00000497830.5:c.*7T>A	ENSP00000420088.1:n.*7T>A
ENST00000497959.5:c.174T>A	ENSP00000420648.1:p.Tyr58Ter
ENST00000539926.5:c.-40T>A	ENSP00000441253.2:n.-40T>A
ENST00000610757.4:c.-40T>A	ENSP00000480435.1:n.-40T>A
ENST00000629669.2:c.174T>A	ENSP00000486824.1:p.Tyr58Ter
XM_006713702.1:c.-40T>A	XP_006713765.1:n.-40T>A
XM_011512992.1:c.174T>A	XP_011511294.1:p.Tyr58Ter
XM_011512992.2:c.174T>A	XP_011511294.1:p.Tyr58Ter
XM_011512993.1:c.288T>A	XP_011511295.1:p.Tyr96Ter
XR_001740207.2:n.411T>A
XR_001740208.2:n.411T>A
XR_001740209.2:n.381T>A
XR_001740210.1:n.241T>A
XR_002959553.1:n.411T>A
XR_002959554.1:n.411T>A
XR_241502.2:n.435T>A
XR_241502.3:n.381T>A
XR_924159.1:n.435T>A