Canonical Allele Identifier: CA2361707811
Gene: FER1L4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.35564917T= , CM000682.2:g.35564917T= GRCh38
NC_000020.10:g.34152833T= , CM000682.1:g.34152833T= GRCh37
NC_000020.9:g.33616247T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000674340.1:n.1975A=
ENST00000674470.1:n.1302A=
ENST00000611673.4:n.996A=
ENST00000613061.4:n.1346A=
ENST00000615531.4:n.4511A=
ENST00000616711.4:n.1660A=
ENST00000621044.4:n.624A=
NR_119376.1:n.4523A=