Canonical Allele Identifier: CA2396892035
Community Standard Title: NM_001017964.2(YDJC):c.787G= (p.Ala263=)
Gene: YDJC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.21628603C= , CM000684.2:g.21628603C= GRCh38
NC_000022.10:g.21982892C= , CM000684.1:g.21982892C= GRCh37
NC_000022.9:g.20312892C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001017964.2:c.787G= MANE Select NP_001017964.1:p.Ala263=
ENST00000292778.11:c.787G= MANE Select ENSP00000292778.6:p.Ala263=
NM_001017964.1:c.787G= NP_001017964.1:p.Ala263=
NM_001371350.1:c.*159G= NP_001358279.1:n.*159G=
NR_163922.1:n.854G=
NR_163923.1:n.676G=
NR_163924.1:n.989G=
NR_163925.1:n.811G=
ENST00000292778.10:c.787G= ENSP00000292778.6:p.Ala263=
ENST00000398873.4:c.*159G= ENSP00000381847.3:n.*159G=
ENST00000415762.6:c.*435G= ENSP00000402481.2:n.*435G=
ENST00000464015.5:n.1099G=
ENST00000468686.5:n.909G=
ENST00000473985.1:n.1005G=
ENST00000482998.1:n.907G=
XM_011529906.1:c.*159G= XP_011528208.1:n.*159G=
XM_011529906.2:c.*159G= XP_011528208.1:n.*159G=
XR_937814.2:n.1115G=