Canonical Allele Identifier: CA519809
Gene: DVL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.1336381G>A , CM000663.2:g.1336381G>A GRCh38
NC_000001.10:g.1271761G>A , CM000663.1:g.1271761G>A GRCh37
NC_000001.9:g.1261624G>A NCBI36
NG_008048.1:g.17732C>T
NG_008048.2:g.17732C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000378888.10:c.1849C>T MANE Select ENSP00000368166.5:p.Arg617Ter
ENST00000378888.9:c.1849C>T ENSP00000368166.5:p.Arg617Ter
ENST00000378891.9:c.1774C>T ENSP00000368169.5:p.Arg592Ter
ENST00000610709.2:c.1096C>T ENSP00000480077.1:p.Arg366Ter
NM_004421.2:c.1774C>T NP_004412.2:p.Arg592Ter
XM_005244731.2:c.1849C>T XP_005244788.1:p.Arg617Ter
NM_001330311.1:c.1849C>T NP_001317240.1:p.Arg617Ter
XM_005244732.4:c.*162C>T XP_005244789.1:n.*162C>T
XM_005244733.4:c.*162C>T XP_005244790.1:n.*162C>T
NM_001330311.2:c.1849C>T MANE Select NP_001317240.1:p.Arg617Ter
NM_004421.3:c.1774C>T NP_004412.2:p.Arg592Ter