Canonical Allele Identifier: CA355319130

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183086691A>G , CM000665.2:g.183086691A>G	GRCh38
NC_000003.11:g.182804479A>G , CM000665.1:g.182804479A>G	GRCh37
NC_000003.10:g.184287173A>G	NCBI36
NG_008100.1:g.17887T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.369+2T>C MANE Select	NP_064551.3:n.369+2T>C
ENST00000265594.9:c.369+2T>C MANE Select	ENSP00000265594.4:n.369+2T>C
NM_001293273.1:c.140+2T>C	NP_001280202.1:n.140+2T>C
NM_001293273.2:c.140+2T>C	NP_001280202.1:n.140+2T>C
NM_001363880.1:c.42+2T>C	NP_001350809.1:n.42+2T>C
NM_020166.4:c.369+2T>C	NP_064551.3:n.369+2T>C
NR_120639.1:n.283+7868T>C
NR_120639.2:n.192+7868T>C
NR_120640.1:n.1036+2T>C
NR_120640.2:n.1036+2T>C
ENST00000265594.8:c.369+2T>C	ENSP00000265594.4:n.369+2T>C
ENST00000466650.5:c.*88+2T>C	ENSP00000418979.1:n.*88+2T>C
ENST00000476176.5:c.228+2T>C	ENSP00000420433.1:n.228+2T>C
ENST00000486226.1:c.*126+2T>C	ENSP00000420223.1:n.*126+2T>C
ENST00000487634.5:c.136+7868T>C	ENSP00000420591.1:n.136+7868T>C
ENST00000490284.5:c.89+12661T>C	ENSP00000419328.1:n.89+12661T>C
ENST00000492597.5:c.42+2T>C	ENSP00000419898.1:n.42+2T>C
ENST00000495767.5:c.136+7868T>C	ENSP00000419658.1:n.136+7868T>C
ENST00000497830.5:c.*88+2T>C	ENSP00000420088.1:n.*88+2T>C
ENST00000497959.5:c.255+2T>C	ENSP00000420648.1:n.255+2T>C
ENST00000539926.5:c.42+2T>C	ENSP00000441253.2:n.42+2T>C
ENST00000610757.4:c.42+2T>C	ENSP00000480435.1:n.42+2T>C
ENST00000629669.2:c.255+2T>C	ENSP00000486824.1:n.255+2T>C
XM_006713702.1:c.42+2T>C	XP_006713765.1:n.42+2T>C
XM_011512992.1:c.255+2T>C	XP_011511294.1:n.255+2T>C
XM_011512992.2:c.255+2T>C	XP_011511294.1:n.255+2T>C
XM_011512993.1:c.369+2T>C	XP_011511295.1:n.369+2T>C
XR_001740207.2:n.492+2T>C
XR_001740208.2:n.492+2T>C
XR_001740209.2:n.462+2T>C
XR_001740210.1:n.322+2T>C
XR_002959553.1:n.492+2T>C
XR_002959554.1:n.492+2T>C
XR_241502.2:n.516+2T>C
XR_241502.3:n.462+2T>C
XR_924159.1:n.516+2T>C