Canonical Allele Identifier: CA355323282

Gene: MCCC1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183041711T>C , CM000665.2:g.183041711T>C	GRCh38
NC_000003.11:g.182759499T>C , CM000665.1:g.182759499T>C	GRCh37
NC_000003.10:g.184242193T>C	NCBI36
NG_008100.1:g.62867A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1123A>G MANE Select	ENSP00000265594.4:p.Ile375Val
ENST00000265594.8:c.1123A>G	ENSP00000265594.4:p.Ile375Val
ENST00000476176.5:c.982A>G	ENSP00000420433.1:p.Ile328Val
ENST00000492597.5:c.796A>G	ENSP00000419898.1:p.Ile266Val
ENST00000495767.5:c.*704A>G	ENSP00000419658.1:n.*704A>G
ENST00000497830.5:c.*720A>G	ENSP00000420088.1:n.*720A>G
ENST00000497959.5:c.1009A>G	ENSP00000420648.1:p.Ile337Val
ENST00000539926.5:c.673A>G	ENSP00000441253.2:p.Ile225Val
ENST00000610757.4:c.673A>G	ENSP00000480435.1:p.Ile225Val
ENST00000629669.2:c.1009A>G	ENSP00000486824.1:p.Ile337Val
NM_001293273.1:c.772A>G	NP_001280202.1:p.Ile258Val
NM_020166.4:c.1123A>G	NP_064551.3:p.Ile375Val
NR_120639.1:n.1037A>G
NR_120640.1:n.1790A>G
XM_006713702.1:c.796A>G	XP_006713765.1:p.Ile266Val
XM_011512992.1:c.1009A>G	XP_011511294.1:p.Ile337Val
XM_011512993.1:c.1123A>G	XP_011511295.1:p.Ile375Val
XR_241502.2:n.1270A>G
XR_924159.1:n.1270A>G
NM_001363880.1:c.796A>G	NP_001350809.1:p.Ile266Val
XM_011512992.2:c.1009A>G	XP_011511294.1:p.Ile337Val
XR_001740207.2:n.1246A>G
XR_001740208.2:n.1246A>G
XR_001740209.2:n.1216A>G
XR_001740210.1:n.1076A>G
XR_002959553.1:n.1246A>G
XR_002959554.1:n.1246A>G
XR_241502.3:n.1216A>G
NM_020166.5:c.1123A>G MANE Select	NP_064551.3:p.Ile375Val
NM_001293273.2:c.772A>G	NP_001280202.1:p.Ile258Val
NR_120639.2:n.946A>G
NR_120640.2:n.1790A>G