Canonical Allele Identifier: CA355321095

Gene: MCCC1

Linked Data

• MyVariant Identifiers: chr3:g.182755213G>C (hg19) ; chr3:g.183037425G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037425G>C , CM000665.2:g.183037425G>C	GRCh38
NC_000003.11:g.182755213G>C , CM000665.1:g.182755213G>C	GRCh37
NC_000003.10:g.184237907G>C	NCBI36
NG_008100.1:g.67153C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1387C>G MANE Select	ENSP00000265594.4:p.Leu463Val
ENST00000265594.8:c.1387C>G	ENSP00000265594.4:p.Leu463Val
ENST00000476176.5:c.1246C>G	ENSP00000420433.1:p.Leu416Val
ENST00000492597.5:c.1060C>G	ENSP00000419898.1:p.Leu354Val
ENST00000495767.5:c.*968C>G	ENSP00000419658.1:n.*968C>G
ENST00000497830.5:c.*984C>G	ENSP00000420088.1:n.*984C>G
ENST00000497959.5:c.1263+1601C>G	ENSP00000420648.1:n.1263+1601C>G
ENST00000539926.5:c.937C>G	ENSP00000441253.2:p.Leu313Val
ENST00000610757.4:c.937C>G	ENSP00000480435.1:p.Leu313Val
ENST00000629669.2:c.1263+1601C>G	ENSP00000486824.1:n.1263+1601C>G
NM_001293273.1:c.1036C>G	NP_001280202.1:p.Leu346Val
NM_020166.4:c.1387C>G	NP_064551.3:p.Leu463Val
NR_120639.1:n.1301C>G
NR_120640.1:n.2044+1601C>G
XM_006713702.1:c.1060C>G	XP_006713765.1:p.Leu354Val
XM_011512992.1:c.1273C>G	XP_011511294.1:p.Leu425Val
XM_011512993.1:c.1377+1601C>G	XP_011511295.1:n.1377+1601C>G
XR_241502.2:n.1524+1601C>G
XR_924159.1:n.1534C>G
NM_001363880.1:c.1060C>G	NP_001350809.1:p.Leu354Val
XM_011512992.2:c.1273C>G	XP_011511294.1:p.Leu425Val
XR_001740207.2:n.1510C>G
XR_001740208.2:n.1510C>G
XR_001740209.2:n.1470+1601C>G
XR_001740210.1:n.1340C>G
XR_002959553.1:n.1510C>G
XR_002959554.1:n.1500+1601C>G
XR_241502.3:n.1470+1601C>G
NM_020166.5:c.1387C>G MANE Select	NP_064551.3:p.Leu463Val
NM_001293273.2:c.1036C>G	NP_001280202.1:p.Leu346Val
NR_120639.2:n.1210C>G
NR_120640.2:n.2044+1601C>G