Canonical Allele Identifier: CA2237143

Gene: RAD18

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.8958938G>T , CM000665.2:g.8958938G>T	GRCh38
NC_000003.11:g.9000622G>T , CM000665.1:g.9000622G>T	GRCh37
NC_000003.10:g.8975622G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264926.7:c.115C>A MANE Select	ENSP00000264926.2:p.Pro39Thr
ENST00000264926.6:c.115C>A	ENSP00000264926.2:p.Pro39Thr
ENST00000413832.1:c.115C>A	ENSP00000412261.1:p.Pro39Thr
ENST00000415439.5:c.115C>A	ENSP00000402049.1:p.Pro39Thr
ENST00000418463.5:c.115C>A	ENSP00000397852.1:p.Pro39Thr
ENST00000421052.5:c.115C>A	ENSP00000399620.1:p.Pro39Thr
ENST00000469793.1:n.173C>A
ENST00000495087.5:n.168+4397C>A
NM_020165.3:c.115C>A	NP_064550.3:p.Pro39Thr
XM_017006873.1:c.-121C>A	XP_016862362.1:n.-121C>A
NM_020165.4:c.115C>A MANE Select	NP_064550.3:p.Pro39Thr