Canonical Allele Identifier: CA1140273008
Gene: ELAVL4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.50094148C= , CM000663.2:g.50094148C= GRCh38
NC_000001.10:g.50559820C= , CM000663.1:g.50559820C= GRCh37
NC_000001.9:g.50332407C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000448907.7:c.18+45966C= ENSP00000399939.2:n.18+45966C=
ENST00000463650.2:c.-13+46424C= ENSP00000498680.1:n.-13+46424C=
ENST00000651693.1:c.-125-3762C= ENSP00000498319.1:n.-125-3762C=
ENST00000652252.1:n.237+26664C=
ENST00000448907.6:c.18+45966C= ENSP00000399939.2:n.18+45966C=
NM_001144777.2:c.18+45966C= NP_001138249.1:n.18+45966C=
XM_011540892.1:c.18+45966C= XP_011539194.1:n.18+45966C=
NM_001324208.1:c.18+45966C= NP_001311137.1:n.18+45966C=
XM_017000542.1:c.18+45966C= XP_016856031.1:n.18+45966C=
NM_001144777.3:c.18+45966C= NP_001138249.1:n.18+45966C=
NM_001324208.2:c.18+45966C= NP_001311137.1:n.18+45966C=