Canonical Allele Identifier: CA337863084

Gene: DVL1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1338522C>T , CM000663.2:g.1338522C>T	GRCh38
NC_000001.10:g.1273902C>T , CM000663.1:g.1273902C>T	GRCh37
NC_000001.9:g.1263765C>T	NCBI36
NG_008048.1:g.15591G>A
NG_008048.2:g.15591G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378888.10:c.1339G>A MANE Select	ENSP00000368166.5:p.Gly447Arg
ENST00000378888.9:c.1339G>A	ENSP00000368166.5:p.Gly447Arg
ENST00000378891.9:c.1264G>A	ENSP00000368169.5:p.Gly422Arg
ENST00000610709.2:c.651-150G>A	ENSP00000480077.1:n.651-150G>A
ENST00000631679.1:c.370G>A	ENSP00000488181.1:p.Gly124Arg
ENST00000632445.1:c.268G>A	ENSP00000488888.1:p.Gly90Arg
ENST00000634054.1:n.725G>A
NM_004421.2:c.1264G>A	NP_004412.2:p.Gly422Arg
XM_005244731.2:c.1339G>A	XP_005244788.1:p.Gly447Arg
XM_005244732.2:c.1339G>A	XP_005244789.1:p.Gly447Arg
XM_005244733.2:c.1264G>A	XP_005244790.1:p.Gly422Arg
NM_001330311.1:c.1339G>A	NP_001317240.1:p.Gly447Arg
XM_005244732.4:c.1339G>A	XP_005244789.1:p.Gly447Arg
XM_005244733.4:c.1264G>A	XP_005244790.1:p.Gly422Arg
NM_001330311.2:c.1339G>A MANE Select	NP_001317240.1:p.Gly447Arg
NM_004421.3:c.1264G>A	NP_004412.2:p.Gly422Arg