Canonical Allele Identifier: CA355319900

Gene: MCCC1

Linked Data

• gnomAD v4: 3-183037238-G-C
• MyVariant Identifiers: chr3:g.182755026G>C (hg19) ; chr3:g.183037238G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037238G>C , CM000665.2:g.183037238G>C	GRCh38
NC_000003.11:g.182755026G>C , CM000665.1:g.182755026G>C	GRCh37
NC_000003.10:g.184237720G>C	NCBI36
NG_008100.1:g.67340C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1574C>G MANE Select	ENSP00000265594.4:p.Thr525Ser
ENST00000265594.8:c.1574C>G	ENSP00000265594.4:p.Thr525Ser
ENST00000476176.5:c.1433C>G	ENSP00000420433.1:p.Thr478Ser
ENST00000489909.1:n.118C>G
ENST00000492597.5:c.1247C>G	ENSP00000419898.1:p.Thr416Ser
ENST00000495767.5:c.*1155C>G	ENSP00000419658.1:n.*1155C>G
ENST00000497830.5:c.*1171C>G	ENSP00000420088.1:n.*1171C>G
ENST00000497959.5:c.1263+1788C>G	ENSP00000420648.1:n.1263+1788C>G
ENST00000539926.5:c.1124C>G	ENSP00000441253.2:p.Thr375Ser
ENST00000610757.4:c.1124C>G	ENSP00000480435.1:p.Thr375Ser
ENST00000629669.2:c.1263+1788C>G	ENSP00000486824.1:n.1263+1788C>G
NM_001293273.1:c.1223C>G	NP_001280202.1:p.Thr408Ser
NM_020166.4:c.1574C>G	NP_064551.3:p.Thr525Ser
NR_120639.1:n.1488C>G
NR_120640.1:n.2044+1788C>G
XM_006713702.1:c.1247C>G	XP_006713765.1:p.Thr416Ser
XM_011512992.1:c.1460C>G	XP_011511294.1:p.Thr487Ser
XM_011512993.1:c.1377+1788C>G	XP_011511295.1:n.1377+1788C>G
XR_241502.2:n.1524+1788C>G
XR_924159.1:n.1721C>G
NM_001363880.1:c.1247C>G	NP_001350809.1:p.Thr416Ser
XM_011512992.2:c.1460C>G	XP_011511294.1:p.Thr487Ser
XR_001740207.2:n.1697C>G
XR_001740208.2:n.1697C>G
XR_001740209.2:n.1470+1788C>G
XR_001740210.1:n.1527C>G
XR_002959553.1:n.1697C>G
XR_002959554.1:n.1500+1788C>G
XR_241502.3:n.1470+1788C>G
NM_020166.5:c.1574C>G MANE Select	NP_064551.3:p.Thr525Ser
NM_001293273.2:c.1223C>G	NP_001280202.1:p.Thr408Ser
NR_120639.2:n.1397C>G
NR_120640.2:n.2044+1788C>G