Canonical Allele Identifier: CA355324098

Gene: MCCC1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.183099351C>T , CM000665.2:g.183099351C>T	GRCh38
NC_000003.11:g.182817139C>T , CM000665.1:g.182817139C>T	GRCh37
NC_000003.10:g.184299833C>T	NCBI36
NG_008100.1:g.5227G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_020166.5:c.89+1G>A MANE Select	NP_064551.3:n.89+1G>A
ENST00000265594.9:c.89+1G>A MANE Select	ENSP00000265594.4:n.89+1G>A
NM_001293273.1:c.-4+1G>A	NP_001280202.1:n.-4+1G>A
NM_001293273.2:c.-4+1G>A	NP_001280202.1:n.-4+1G>A
NM_001363880.1:c.-102+1G>A	NP_001350809.1:n.-102+1G>A
NM_020166.4:c.89+1G>A	NP_064551.3:n.89+1G>A
NR_120639.1:n.236+1G>A
NR_120639.2:n.145+1G>A
ENST00000265594.8:c.89+1G>A	ENSP00000265594.4:n.89+1G>A
ENST00000466650.5:c.89+1G>A	ENSP00000418979.1:n.89+1G>A
ENST00000476176.5:c.89+1G>A	ENSP00000420433.1:n.89+1G>A
ENST00000486226.1:c.89+1G>A	ENSP00000420223.1:n.89+1G>A
ENST00000487634.5:c.89+1G>A	ENSP00000420591.1:n.89+1G>A
ENST00000490284.5:c.89+1G>A	ENSP00000419328.1:n.89+1G>A
ENST00000492597.5:c.-101-4746G>A	ENSP00000419898.1:n.-101-4746G>A
ENST00000495767.5:c.89+1G>A	ENSP00000419658.1:n.89+1G>A
ENST00000497830.5:c.89+1G>A	ENSP00000420088.1:n.89+1G>A
ENST00000539926.5:c.-102+1G>A	ENSP00000441253.2:n.-102+1G>A
ENST00000610757.4:c.-239+1G>A	ENSP00000480435.1:n.-239+1G>A
ENST00000629669.2:c.-26+1G>A	ENSP00000486824.1:n.-26+1G>A
XM_006713702.1:c.-102+1G>A	XP_006713765.1:n.-102+1G>A
XM_011512993.1:c.89+1G>A	XP_011511295.1:n.89+1G>A
XR_001740207.2:n.212+1G>A
XR_001740208.2:n.212+1G>A
XR_001740209.2:n.182+1G>A
XR_001740210.1:n.179+1G>A
XR_002959553.1:n.212+1G>A
XR_002959554.1:n.212+1G>A
XR_241502.2:n.236+1G>A
XR_241502.3:n.182+1G>A
XR_924159.1:n.236+1G>A