Canonical Allele Identifier: CA10521251

Gene: PHF6

Linked Data

• dbSNP Id: rs201922281
• ExAC: X:133548995 TTCTC / T
• gnomAD v2: X-133548995-TTCTC-T
• gnomAD v3: X-134414965-TTCTC-T
• gnomAD v4: X-134414965-TTCTC-T
• COSMIC: COSN17149141
• MyVariant Identifiers: chrX:g.133548996_133548999del (hg19) ; chrX:g.133548998_133549001delTCTC (hg19) ; chrX:g.134414967_134414970del (hg38) ; chrX:g.134414966_134414969del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134414968_134414971del , CM000685.2:g.134414968_134414971del	GRCh38
NC_000023.10:g.133548998_133549001del , CM000685.1:g.133548998_133549001del	GRCh37
NC_000023.9:g.133376664_133376667del	NCBI36
NG_008886.1:g.46657_46660del , LRG_629:g.46657_46660del

Transcript Alleles

HGVS	Amino-acid change
ENST00000685553.1:c.*649-48_*649-45del	ENSP00000510193.1:n.*649-48_*649-45del
ENST00000687496.1:c.628-48_628-45del	ENSP00000509551.1:n.628-48_628-45del
ENST00000688598.1:c.628-48_628-45del	ENSP00000510410.1:n.628-48_628-45del
ENST00000691812.1:c.730-48_730-45del	ENSP00000510211.1:n.730-48_730-45del
ENST00000693759.1:c.*342-48_*342-45del	ENSP00000509518.1:n.*342-48_*342-45del
ENST00000370803.8:c.730-48_730-45del MANE Select	ENSP00000359839.4:n.730-48_730-45del
ENST00000332070.7:c.730-48_730-45del	ENSP00000329097.3:n.730-48_730-45del
ENST00000370799.5:c.733-48_733-45del	ENSP00000359835.1:n.733-48_733-45del
ENST00000370800.4:c.733-48_733-45del	ENSP00000359836.4:n.733-48_733-45del
ENST00000370803.7:c.730-48_730-45del	ENSP00000359839.3:n.730-48_730-45del
ENST00000625464.2:c.733-48_733-45del	ENSP00000487420.1:n.733-48_733-45del
NM_001015877.1:c.730-48_730-45del , LRG_629t1:c.730-48_730-45del	NP_001015877.1:n.730-48_730-45del
NM_032335.3:c.733-48_733-45del , LRG_629t2:c.733-48_733-45del	NP_115711.2:n.733-48_733-45del
NM_032458.2:c.730-48_730-45del	NP_115834.1:n.730-48_730-45del
NM_001015877.2:c.730-48_730-45del MANE Select	NP_001015877.1:n.730-48_730-45del
NM_032458.3:c.730-48_730-45del	NP_115834.1:n.730-48_730-45del