Canonical Allele Identifier: CA355321932

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182756863T>A (hg19) ; chr3:g.183039075T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039075T>A , CM000665.2:g.183039075T>A	GRCh38
NC_000003.11:g.182756863T>A , CM000665.1:g.182756863T>A	GRCh37
NC_000003.10:g.184239557T>A	NCBI36
NG_008100.1:g.65503A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1328A>T MANE Select	ENSP00000265594.4:p.Asp443Val
ENST00000265594.8:c.1328A>T	ENSP00000265594.4:p.Asp443Val
ENST00000476176.5:c.1187A>T	ENSP00000420433.1:p.Asp396Val
ENST00000492597.5:c.1001A>T	ENSP00000419898.1:p.Asp334Val
ENST00000495767.5:c.*909A>T	ENSP00000419658.1:n.*909A>T
ENST00000497830.5:c.*925A>T	ENSP00000420088.1:n.*925A>T
ENST00000497959.5:c.1214A>T	ENSP00000420648.1:p.Asp405Val
ENST00000539926.5:c.878A>T	ENSP00000441253.2:p.Asp293Val
ENST00000610757.4:c.878A>T	ENSP00000480435.1:p.Asp293Val
ENST00000629669.2:c.1214A>T	ENSP00000486824.1:p.Asp405Val
NM_001293273.1:c.977A>T	NP_001280202.1:p.Asp326Val
NM_020166.4:c.1328A>T	NP_064551.3:p.Asp443Val
NR_120639.1:n.1242A>T
NR_120640.1:n.1995A>T
XM_006713702.1:c.1001A>T	XP_006713765.1:p.Asp334Val
XM_011512992.1:c.1214A>T	XP_011511294.1:p.Asp405Val
XM_011512993.1:c.1328A>T	XP_011511295.1:p.Asp443Val
XR_241502.2:n.1475A>T
XR_924159.1:n.1475A>T
NM_001363880.1:c.1001A>T	NP_001350809.1:p.Asp334Val
XM_011512992.2:c.1214A>T	XP_011511294.1:p.Asp405Val
XR_001740207.2:n.1451A>T
XR_001740208.2:n.1451A>T
XR_001740209.2:n.1421A>T
XR_001740210.1:n.1281A>T
XR_002959553.1:n.1451A>T
XR_002959554.1:n.1451A>T
XR_241502.3:n.1421A>T
NM_020166.5:c.1328A>T MANE Select	NP_064551.3:p.Asp443Val
NM_001293273.2:c.977A>T	NP_001280202.1:p.Asp326Val
NR_120639.2:n.1151A>T
NR_120640.2:n.1995A>T