Canonical Allele Identifier: CA355318206

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183033989A>G , CM000665.2:g.183033989A>G	GRCh38
NC_000003.11:g.182751777A>G , CM000665.1:g.182751777A>G	GRCh37
NC_000003.10:g.184234471A>G	NCBI36
NG_008100.1:g.70589T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.1681+2T>C MANE Select	NP_064551.3:n.1681+2T>C
ENST00000265594.9:c.1681+2T>C MANE Select	ENSP00000265594.4:n.1681+2T>C
NM_001293273.1:c.1330+2T>C	NP_001280202.1:n.1330+2T>C
NM_001293273.2:c.1330+2T>C	NP_001280202.1:n.1330+2T>C
NM_001363880.1:c.1354+2T>C	NP_001350809.1:n.1354+2T>C
NM_020166.4:c.1681+2T>C	NP_064551.3:n.1681+2T>C
NR_120639.1:n.1595+2T>C
NR_120639.2:n.1504+2T>C
NR_120640.1:n.2131+2T>C
NR_120640.2:n.2131+2T>C
ENST00000265594.8:c.1681+2T>C	ENSP00000265594.4:n.1681+2T>C
ENST00000476176.5:c.1540+2T>C	ENSP00000420433.1:n.1540+2T>C
ENST00000489909.1:n.225+2T>C
ENST00000492597.5:c.1354+2T>C	ENSP00000419898.1:n.1354+2T>C
ENST00000495767.5:c.*1262+2T>C	ENSP00000419658.1:n.*1262+2T>C
ENST00000497830.5:c.*1278+2T>C	ENSP00000420088.1:n.*1278+2T>C
ENST00000497959.5:c.*45+2T>C	ENSP00000420648.1:n.*45+2T>C
ENST00000539926.5:c.1231+2T>C	ENSP00000441253.2:n.1231+2T>C
ENST00000610757.4:c.1231+2T>C	ENSP00000480435.1:n.1231+2T>C
ENST00000629669.2:c.*45+2T>C	ENSP00000486824.1:n.*45+2T>C
XM_006713702.1:c.1354+2T>C	XP_006713765.1:n.1354+2T>C
XM_011512992.1:c.1567+2T>C	XP_011511294.1:n.1567+2T>C
XM_011512992.2:c.1567+2T>C	XP_011511294.1:n.1567+2T>C
XM_011512993.1:c.*45+2T>C	XP_011511295.1:n.*45+2T>C
XR_001740207.2:n.1804+2T>C
XR_001740208.2:n.1804+2T>C
XR_001740209.2:n.1557+2T>C
XR_001740210.1:n.1634+2T>C
XR_002959553.1:n.1806T>C
XR_002959554.1:n.1587+2T>C
XR_241502.2:n.1611+2T>C
XR_241502.3:n.1557+2T>C
XR_924159.1:n.1828+2T>C