Canonical Allele Identifier: CA355322442

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183094572G>T , CM000665.2:g.183094572G>T	GRCh38
NC_000003.11:g.182812360G>T , CM000665.1:g.182812360G>T	GRCh37
NC_000003.10:g.184295054G>T	NCBI36
NG_008100.1:g.10006C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.123C>A MANE Select	NP_064551.3:p.Tyr41Ter
ENST00000265594.9:c.123C>A MANE Select	ENSP00000265594.4:p.Tyr41Ter
NM_001293273.1:c.31C>A	NP_001280202.1:p.His11Asn
NM_001293273.2:c.31C>A	NP_001280202.1:p.His11Asn
NM_001363880.1:c.-68C>A	NP_001350809.1:n.-68C>A
NM_020166.4:c.123C>A	NP_064551.3:p.Tyr41Ter
NR_120639.1:n.270C>A
NR_120639.2:n.179C>A
NR_120640.1:n.790C>A
NR_120640.2:n.790C>A
ENST00000265594.8:c.123C>A	ENSP00000265594.4:p.Tyr41Ter
ENST00000466650.5:c.123C>A	ENSP00000418979.1:p.Tyr41Ter
ENST00000473955.1:n.36C>A
ENST00000476176.5:c.123C>A	ENSP00000420433.1:p.Tyr41Ter
ENST00000486226.1:c.123C>A	ENSP00000420223.1:p.Tyr41Ter
ENST00000487634.5:c.123C>A	ENSP00000420591.1:p.Tyr41Ter
ENST00000490284.5:c.89+4780C>A	ENSP00000419328.1:n.89+4780C>A
ENST00000492597.5:c.-68C>A	ENSP00000419898.1:n.-68C>A
ENST00000495767.5:c.123C>A	ENSP00000419658.1:p.Tyr41Ter
ENST00000497830.5:c.123C>A	ENSP00000420088.1:p.Tyr41Ter
ENST00000497959.5:c.9C>A	ENSP00000420648.1:p.Tyr3Ter
ENST00000539926.5:c.-68C>A	ENSP00000441253.2:n.-68C>A
ENST00000610757.4:c.-205C>A	ENSP00000480435.1:n.-205C>A
ENST00000629669.2:c.9C>A	ENSP00000486824.1:p.Tyr3Ter
XM_006713702.1:c.-68C>A	XP_006713765.1:n.-68C>A
XM_011512992.1:c.9C>A	XP_011511294.1:p.Tyr3Ter
XM_011512992.2:c.9C>A	XP_011511294.1:p.Tyr3Ter
XM_011512993.1:c.123C>A	XP_011511295.1:p.Tyr41Ter
XR_001740207.2:n.246C>A
XR_001740208.2:n.246C>A
XR_001740209.2:n.216C>A
XR_001740210.1:n.213C>A
XR_002959553.1:n.246C>A
XR_002959554.1:n.246C>A
XR_241502.2:n.270C>A
XR_241502.3:n.216C>A
XR_924159.1:n.270C>A