Canonical Allele Identifier: CA355321764

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182756819A>T (hg19) ; chr3:g.183039031A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039031A>T , CM000665.2:g.183039031A>T	GRCh38
NC_000003.11:g.182756819A>T , CM000665.1:g.182756819A>T	GRCh37
NC_000003.10:g.184239513A>T	NCBI36
NG_008100.1:g.65547T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000265594.9:c.1372T>A MANE Select	ENSP00000265594.4:p.Tyr458Asn
ENST00000265594.8:c.1372T>A	ENSP00000265594.4:p.Tyr458Asn
ENST00000476176.5:c.1231T>A	ENSP00000420433.1:p.Tyr411Asn
ENST00000492597.5:c.1045T>A	ENSP00000419898.1:p.Tyr349Asn
ENST00000495767.5:c.*953T>A	ENSP00000419658.1:n.*953T>A
ENST00000497830.5:c.*969T>A	ENSP00000420088.1:n.*969T>A
ENST00000497959.5:c.1258T>A	ENSP00000420648.1:p.Tyr420Asn
ENST00000539926.5:c.922T>A	ENSP00000441253.2:p.Tyr308Asn
ENST00000610757.4:c.922T>A	ENSP00000480435.1:p.Tyr308Asn
ENST00000629669.2:c.1258T>A	ENSP00000486824.1:p.Tyr420Asn
NM_001293273.1:c.1021T>A	NP_001280202.1:p.Tyr341Asn
NM_020166.4:c.1372T>A	NP_064551.3:p.Tyr458Asn
NR_120639.1:n.1286T>A
NR_120640.1:n.2039T>A
XM_006713702.1:c.1045T>A	XP_006713765.1:p.Tyr349Asn
XM_011512992.1:c.1258T>A	XP_011511294.1:p.Tyr420Asn
XM_011512993.1:c.1372T>A	XP_011511295.1:p.Tyr458Asn
XR_241502.2:n.1519T>A
XR_924159.1:n.1519T>A
NM_001363880.1:c.1045T>A	NP_001350809.1:p.Tyr349Asn
XM_011512992.2:c.1258T>A	XP_011511294.1:p.Tyr420Asn
XR_001740207.2:n.1495T>A
XR_001740208.2:n.1495T>A
XR_001740209.2:n.1465T>A
XR_001740210.1:n.1325T>A
XR_002959553.1:n.1495T>A
XR_002959554.1:n.1495T>A
XR_241502.3:n.1465T>A
NM_020166.5:c.1372T>A MANE Select	NP_064551.3:p.Tyr458Asn
NM_001293273.2:c.1021T>A	NP_001280202.1:p.Tyr341Asn
NR_120639.2:n.1195T>A
NR_120640.2:n.2039T>A