Canonical Allele Identifier: CA337878969
Gene: DVL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1348901G>T , CM000663.2:g.1348901G>T GRCh38
NC_000001.10:g.1284281G>T , CM000663.1:g.1284281G>T GRCh37
NC_000001.9:g.1274144G>T NCBI36
NG_008048.1:g.5212C>A
NG_008048.2:g.5212C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000378888.10:c.165C>A MANE Select ENSP00000368166.5:p.Asp55Glu
ENST00000378888.9:c.165C>A ENSP00000368166.5:p.Asp55Glu
ENST00000378891.9:c.165C>A ENSP00000368169.5:p.Asp55Glu
ENST00000472445.1:n.55C>A
ENST00000610709.2:c.165C>A ENSP00000480077.1:p.Asp55Glu
NM_004421.2:c.165C>A NP_004412.2:p.Asp55Glu
XM_005244731.2:c.165C>A XP_005244788.1:p.Asp55Glu
XM_005244732.2:c.165C>A XP_005244789.1:p.Asp55Glu
XM_005244733.2:c.165C>A XP_005244790.1:p.Asp55Glu
NM_001330311.1:c.165C>A NP_001317240.1:p.Asp55Glu
XM_005244732.4:c.165C>A XP_005244789.1:p.Asp55Glu
XM_005244733.4:c.165C>A XP_005244790.1:p.Asp55Glu
NM_001330311.2:c.165C>A MANE Select NP_001317240.1:p.Asp55Glu
NM_004421.3:c.165C>A NP_004412.2:p.Asp55Glu