Canonical Allele Identifier: CA871929558

Gene: TM9SF5P

Linked Data

• dbSNP Id: rs1295257709
• MyVariant Identifiers: chrX:g.136055277G>T (hg19) ; chrX:g.136973118G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136973118G>T , CM000685.2:g.136973118G>T	GRCh38
NC_000023.10:g.136055277G>T , CM000685.1:g.136055277G>T	GRCh37
NC_000023.9:g.135882943G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000431464.6:n.521+47739G>T
ENST00000650669.2:n.413-48294G>T
ENST00000685550.1:n.389-29207G>T
ENST00000685929.1:n.389-20368G>T
ENST00000686432.1:n.459-48294G>T
ENST00000687469.1:n.399-20368G>T
ENST00000687978.1:n.829+47739G>T
ENST00000688713.1:n.365-21729G>T
ENST00000693626.1:n.357+63338G>T
ENST00000693698.1:n.581-21729G>T
ENST00000650669.1:n.413-48294G>T
ENST00000424306.5:n.2053-20368G>T
ENST00000426943.4:n.463+9667G>T
ENST00000431464.5:n.439+47739G>T