Canonical Allele Identifier: CA644639250

Gene: TM9SF5P

Linked Data

• dbSNP Id: rs1301874465
• gnomAD v2: X-136055259-CAA-C
• MyVariant Identifiers: chrX:g.136055260_136055261del (hg19) ; chrX:g.136973101_136973102del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136973101_136973102del , CM000685.2:g.136973101_136973102del	GRCh38
NC_000023.10:g.136055260_136055261del , CM000685.1:g.136055260_136055261del	GRCh37
NC_000023.9:g.135882926_135882927del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000431464.6:n.521+47722_521+47723del
ENST00000650669.2:n.413-48311_413-48310del
ENST00000685550.1:n.389-29224_389-29223del
ENST00000685929.1:n.389-20385_389-20384del
ENST00000686432.1:n.459-48311_459-48310del
ENST00000687469.1:n.399-20385_399-20384del
ENST00000687978.1:n.829+47722_829+47723del
ENST00000688713.1:n.365-21746_365-21745del
ENST00000693626.1:n.357+63321_357+63322del
ENST00000693698.1:n.581-21746_581-21745del
ENST00000650669.1:n.413-48311_413-48310del
ENST00000424306.5:n.2053-20385_2053-20384del
ENST00000426943.4:n.463+9650_463+9651del
ENST00000431464.5:n.439+47722_439+47723del