Canonical Allele Identifier: CA2718775

Gene: MCCC1

Linked Data

• ClinVar Variation Id: 1101705
• ClinVar RCV Id: RCV001424740
• dbSNP Id: rs200216718
• ExAC: 3:182755151 G / A
• gnomAD v2: 3-182755151-G-A
• gnomAD v3: 3-183037363-G-A
• gnomAD v4: 3-183037363-G-A
• MyVariant Identifiers: chr3:g.182755151G>A (hg19) ; chr3:g.183037363G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037363G>A , CM000665.2:g.183037363G>A	GRCh38
NC_000003.11:g.182755151G>A , CM000665.1:g.182755151G>A	GRCh37
NC_000003.10:g.184237845G>A	NCBI36
NG_008100.1:g.67215C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1449C>T MANE Select	ENSP00000265594.4:p.Asn483=
ENST00000265594.8:c.1449C>T	ENSP00000265594.4:p.Asn483=
ENST00000476176.5:c.1308C>T	ENSP00000420433.1:p.Asn436=
ENST00000492597.5:c.1122C>T	ENSP00000419898.1:p.Asn374=
ENST00000495767.5:c.*1030C>T	ENSP00000419658.1:n.*1030C>T
ENST00000497830.5:c.*1046C>T	ENSP00000420088.1:n.*1046C>T
ENST00000497959.5:c.1263+1663C>T	ENSP00000420648.1:n.1263+1663C>T
ENST00000539926.5:c.999C>T	ENSP00000441253.2:p.Asn333=
ENST00000610757.4:c.999C>T	ENSP00000480435.1:p.Asn333=
ENST00000629669.2:c.1263+1663C>T	ENSP00000486824.1:n.1263+1663C>T
NM_001293273.1:c.1098C>T	NP_001280202.1:p.Asn366=
NM_020166.4:c.1449C>T	NP_064551.3:p.Asn483=
NR_120639.1:n.1363C>T
NR_120640.1:n.2044+1663C>T
XM_006713702.1:c.1122C>T	XP_006713765.1:p.Asn374=
XM_011512992.1:c.1335C>T	XP_011511294.1:p.Asn445=
XM_011512993.1:c.1377+1663C>T	XP_011511295.1:n.1377+1663C>T
XR_241502.2:n.1524+1663C>T
XR_924159.1:n.1596C>T
NM_001363880.1:c.1122C>T	NP_001350809.1:p.Asn374=
XM_011512992.2:c.1335C>T	XP_011511294.1:p.Asn445=
XR_001740207.2:n.1572C>T
XR_001740208.2:n.1572C>T
XR_001740209.2:n.1470+1663C>T
XR_001740210.1:n.1402C>T
XR_002959553.1:n.1572C>T
XR_002959554.1:n.1500+1663C>T
XR_241502.3:n.1470+1663C>T
NM_020166.5:c.1449C>T MANE Select	NP_064551.3:p.Asn483=
NM_001293273.2:c.1098C>T	NP_001280202.1:p.Asn366=
NR_120639.2:n.1272C>T
NR_120640.2:n.2044+1663C>T