Canonical Allele Identifier: CA88702156

Gene: MCCC1

Linked Data

• dbSNP Id: rs1001495052
• MyVariant Identifiers: chr3:g.182756906G>A (hg19) ; chr3:g.183039118G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183039118G>A , CM000665.2:g.183039118G>A	GRCh38
NC_000003.11:g.182756906G>A , CM000665.1:g.182756906G>A	GRCh37
NC_000003.10:g.184239600G>A	NCBI36
NG_008100.1:g.65460C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1285C>T MANE Select	ENSP00000265594.4:p.His429Tyr
ENST00000265594.8:c.1285C>T	ENSP00000265594.4:p.His429Tyr
ENST00000476176.5:c.1144C>T	ENSP00000420433.1:p.His382Tyr
ENST00000492597.5:c.958C>T	ENSP00000419898.1:p.His320Tyr
ENST00000495767.5:c.*866C>T	ENSP00000419658.1:n.*866C>T
ENST00000497830.5:c.*882C>T	ENSP00000420088.1:n.*882C>T
ENST00000497959.5:c.1171C>T	ENSP00000420648.1:p.His391Tyr
ENST00000539926.5:c.835C>T	ENSP00000441253.2:p.His279Tyr
ENST00000610757.4:c.835C>T	ENSP00000480435.1:p.His279Tyr
ENST00000629669.2:c.1171C>T	ENSP00000486824.1:p.His391Tyr
NM_001293273.1:c.934C>T	NP_001280202.1:p.His312Tyr
NM_020166.4:c.1285C>T	NP_064551.3:p.His429Tyr
NR_120639.1:n.1199C>T
NR_120640.1:n.1952C>T
XM_006713702.1:c.958C>T	XP_006713765.1:p.His320Tyr
XM_011512992.1:c.1171C>T	XP_011511294.1:p.His391Tyr
XM_011512993.1:c.1285C>T	XP_011511295.1:p.His429Tyr
XR_241502.2:n.1432C>T
XR_924159.1:n.1432C>T
NM_001363880.1:c.958C>T	NP_001350809.1:p.His320Tyr
XM_011512992.2:c.1171C>T	XP_011511294.1:p.His391Tyr
XR_001740207.2:n.1408C>T
XR_001740208.2:n.1408C>T
XR_001740209.2:n.1378C>T
XR_001740210.1:n.1238C>T
XR_002959553.1:n.1408C>T
XR_002959554.1:n.1408C>T
XR_241502.3:n.1378C>T
NM_020166.5:c.1285C>T MANE Select	NP_064551.3:p.His429Tyr
NM_001293273.2:c.934C>T	NP_001280202.1:p.His312Tyr
NR_120639.2:n.1108C>T
NR_120640.2:n.1952C>T