Canonical Allele Identifier: CA519803
Community Standard Title: NM_001330311.2(DVL1):c.1855C>T (p.Arg619Cys)
Gene: DVL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1336375G>A , CM000663.2:g.1336375G>A GRCh38
NC_000001.10:g.1271755G>A , CM000663.1:g.1271755G>A GRCh37
NC_000001.9:g.1261618G>A NCBI36
NG_008048.1:g.17738C>T
NG_008048.2:g.17738C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001330311.2:c.1855C>T MANE Select NP_001317240.1:p.Arg619Cys
ENST00000378888.10:c.1855C>T MANE Select ENSP00000368166.5:p.Arg619Cys
NM_001330311.1:c.1855C>T NP_001317240.1:p.Arg619Cys
NM_004421.2:c.1780C>T NP_004412.2:p.Arg594Cys
NM_004421.3:c.1780C>T NP_004412.2:p.Arg594Cys
ENST00000378888.9:c.1855C>T ENSP00000368166.5:p.Arg619Cys
ENST00000378891.9:c.1780C>T ENSP00000368169.5:p.Arg594Cys
ENST00000610709.2:c.1102C>T ENSP00000480077.1:p.Arg368Cys
XM_005244731.2:c.1855C>T XP_005244788.1:p.Arg619Cys
XM_005244732.4:c.*168C>T XP_005244789.1:n.*168C>T
XM_005244733.4:c.*168C>T XP_005244790.1:n.*168C>T