Canonical Allele Identifier: CA648594658

Gene: MCCC1

Linked Data

• COSMIC: COSN1935602

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183042266C>T , CM000665.2:g.183042266C>T	GRCh38
NC_000003.11:g.182760054C>T , CM000665.1:g.182760054C>T	GRCh37
NC_000003.10:g.184242748C>T	NCBI36
NG_008100.1:g.62312G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265594.9:c.1084-516G>A MANE Select	ENSP00000265594.4:n.1084-516G>A
ENST00000265594.8:c.1084-516G>A	ENSP00000265594.4:n.1084-516G>A
ENST00000476176.5:c.943-516G>A	ENSP00000420433.1:n.943-516G>A
ENST00000492597.5:c.757-516G>A	ENSP00000419898.1:n.757-516G>A
ENST00000495767.5:c.*665-516G>A	ENSP00000419658.1:n.*665-516G>A
ENST00000497830.5:c.*681-516G>A	ENSP00000420088.1:n.*681-516G>A
ENST00000497959.5:c.970-516G>A	ENSP00000420648.1:n.970-516G>A
ENST00000539926.5:c.634-516G>A	ENSP00000441253.2:n.634-516G>A
ENST00000610757.4:c.634-516G>A	ENSP00000480435.1:n.634-516G>A
ENST00000629669.2:c.970-516G>A	ENSP00000486824.1:n.970-516G>A
NM_001293273.1:c.733-516G>A	NP_001280202.1:n.733-516G>A
NM_020166.4:c.1084-516G>A	NP_064551.3:n.1084-516G>A
NR_120639.1:n.998-516G>A
NR_120640.1:n.1751-516G>A
XM_006713702.1:c.757-516G>A	XP_006713765.1:n.757-516G>A
XM_011512992.1:c.970-516G>A	XP_011511294.1:n.970-516G>A
XM_011512993.1:c.1084-516G>A	XP_011511295.1:n.1084-516G>A
XR_241502.2:n.1231-516G>A
XR_924159.1:n.1231-516G>A
NM_001363880.1:c.757-516G>A	NP_001350809.1:n.757-516G>A
XM_011512992.2:c.970-516G>A	XP_011511294.1:n.970-516G>A
XR_001740207.2:n.1207-516G>A
XR_001740208.2:n.1207-516G>A
XR_001740209.2:n.1177-516G>A
XR_001740210.1:n.1037-516G>A
XR_002959553.1:n.1207-516G>A
XR_002959554.1:n.1207-516G>A
XR_241502.3:n.1177-516G>A
NM_020166.5:c.1084-516G>A MANE Select	NP_064551.3:n.1084-516G>A
NM_001293273.2:c.733-516G>A	NP_001280202.1:n.733-516G>A
NR_120639.2:n.907-516G>A
NR_120640.2:n.1751-516G>A