Canonical Allele Identifier: CA903587822

Gene: MCCC1

Linked Data

• dbSNP Id: rs1308203447
• gnomAD v3: 3-183037201-A-G
• gnomAD v4: 3-183037201-A-G
• MyVariant Identifiers: chr3:g.182754989A>G (hg19) ; chr3:g.183037201A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183037201A>G , CM000665.2:g.183037201A>G	GRCh38
NC_000003.11:g.182754989A>G , CM000665.1:g.182754989A>G	GRCh37
NC_000003.10:g.184237683A>G	NCBI36
NG_008100.1:g.67377T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1594+17T>C MANE Select	ENSP00000265594.4:n.1594+17T>C
ENST00000265594.8:c.1594+17T>C	ENSP00000265594.4:n.1594+17T>C
ENST00000476176.5:c.1453+17T>C	ENSP00000420433.1:n.1453+17T>C
ENST00000489909.1:n.138+17T>C
ENST00000492597.5:c.1267+17T>C	ENSP00000419898.1:n.1267+17T>C
ENST00000495767.5:c.*1175+17T>C	ENSP00000419658.1:n.*1175+17T>C
ENST00000497830.5:c.*1191+17T>C	ENSP00000420088.1:n.*1191+17T>C
ENST00000497959.5:c.1263+1825T>C	ENSP00000420648.1:n.1263+1825T>C
ENST00000539926.5:c.1144+17T>C	ENSP00000441253.2:n.1144+17T>C
ENST00000610757.4:c.1144+17T>C	ENSP00000480435.1:n.1144+17T>C
ENST00000629669.2:c.1263+1825T>C	ENSP00000486824.1:n.1263+1825T>C
NM_001293273.1:c.1243+17T>C	NP_001280202.1:n.1243+17T>C
NM_020166.4:c.1594+17T>C	NP_064551.3:n.1594+17T>C
NR_120639.1:n.1508+17T>C
NR_120640.1:n.2044+1825T>C
XM_006713702.1:c.1267+17T>C	XP_006713765.1:n.1267+17T>C
XM_011512992.1:c.1480+17T>C	XP_011511294.1:n.1480+17T>C
XM_011512993.1:c.1377+1825T>C	XP_011511295.1:n.1377+1825T>C
XR_241502.2:n.1524+1825T>C
XR_924159.1:n.1741+17T>C
NM_001363880.1:c.1267+17T>C	NP_001350809.1:n.1267+17T>C
XM_011512992.2:c.1480+17T>C	XP_011511294.1:n.1480+17T>C
XR_001740207.2:n.1717+17T>C
XR_001740208.2:n.1717+17T>C
XR_001740209.2:n.1470+1825T>C
XR_001740210.1:n.1547+17T>C
XR_002959553.1:n.1717+17T>C
XR_002959554.1:n.1500+1825T>C
XR_241502.3:n.1470+1825T>C
NM_020166.5:c.1594+17T>C MANE Select	NP_064551.3:n.1594+17T>C
NM_001293273.2:c.1243+17T>C	NP_001280202.1:n.1243+17T>C
NR_120639.2:n.1417+17T>C
NR_120640.2:n.2044+1825T>C