Canonical Allele Identifier: CA410813013
Community Standard Title: NM_001017964.2(YDJC):c.787G>T (p.Ala263Ser)
Gene: YDJC HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_001017964.2:c.787G>T MANE Select NP_001017964.1:p.Ala263Ser
ENST00000292778.11:c.787G>T MANE Select ENSP00000292778.6:p.Ala263Ser
NM_001017964.1:c.787G>T NP_001017964.1:p.Ala263Ser
NM_001371350.1:c.*159G>T NP_001358279.1:n.*159G>T
NR_163922.1:n.854G>T
NR_163923.1:n.676G>T
NR_163924.1:n.989G>T
NR_163925.1:n.811G>T
ENST00000292778.10:c.787G>T ENSP00000292778.6:p.Ala263Ser
ENST00000398873.4:c.*159G>T ENSP00000381847.3:n.*159G>T
ENST00000415762.6:c.*435G>T ENSP00000402481.2:n.*435G>T
ENST00000464015.5:n.1099G>T
ENST00000468686.5:n.909G>T
ENST00000473985.1:n.1005G>T
ENST00000482998.1:n.907G>T
XM_011529906.1:c.*159G>T XP_011528208.1:n.*159G>T
XM_011529906.2:c.*159G>T XP_011528208.1:n.*159G>T
XR_937814.2:n.1115G>T