Canonical Allele Identifier: CA2460521019
Gene: TM9SF5P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.136973088C= , CM000685.2:g.136973088C= GRCh38
NC_000023.10:g.136055247C= , CM000685.1:g.136055247C= GRCh37
NC_000023.9:g.135882913C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000431464.6:n.521+47709C=
ENST00000650669.2:n.413-48324C=
ENST00000685550.1:n.389-29237C=
ENST00000685929.1:n.389-20398C=
ENST00000686432.1:n.459-48324C=
ENST00000687469.1:n.399-20398C=
ENST00000687978.1:n.829+47709C=
ENST00000688713.1:n.365-21759C=
ENST00000693626.1:n.357+63308C=
ENST00000693698.1:n.581-21759C=
ENST00000650669.1:n.413-48324C=
ENST00000424306.5:n.2053-20398C=
ENST00000426943.4:n.463+9637C=
ENST00000431464.5:n.439+47709C=