Canonical Allele Identifier: CA2694738300

Gene: PHF6

Linked Data

• gnomAD v4: X-134414049-ATT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134414058_134414059del , CM000685.2:g.134414058_134414059del	GRCh38
NC_000023.10:g.133548088_133548089del , CM000685.1:g.133548088_133548089del	GRCh37
NC_000023.9:g.133375754_133375755del	NCBI36
NG_008886.1:g.45747_45748del , LRG_629:g.45747_45748del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685553.1:c.*648+92_*648+93del	ENSP00000510193.1:n.*648+92_*648+93del
ENST00000687496.1:c.627+92_627+93del	ENSP00000509551.1:n.627+92_627+93del
ENST00000688598.1:c.627+92_627+93del	ENSP00000510410.1:n.627+92_627+93del
ENST00000691812.1:c.729+92_729+93del	ENSP00000510211.1:n.729+92_729+93del
ENST00000693759.1:c.*341+92_*341+93del	ENSP00000509518.1:n.*341+92_*341+93del
ENST00000370803.8:c.729+92_729+93del MANE Select	ENSP00000359839.4:n.729+92_729+93del
ENST00000332070.7:c.729+92_729+93del	ENSP00000329097.3:n.729+92_729+93del
ENST00000370799.5:c.732+92_732+93del	ENSP00000359835.1:n.732+92_732+93del
ENST00000370800.4:c.732+92_732+93del	ENSP00000359836.4:n.732+92_732+93del
ENST00000370803.7:c.729+92_729+93del	ENSP00000359839.3:n.729+92_729+93del
ENST00000625464.2:c.732+92_732+93del	ENSP00000487420.1:n.732+92_732+93del
NM_001015877.1:c.729+92_729+93del , LRG_629t1:c.729+92_729+93del	NP_001015877.1:n.729+92_729+93del
NM_032335.3:c.732+92_732+93del , LRG_629t2:c.732+92_732+93del	NP_115711.2:n.732+92_732+93del
NM_032458.2:c.729+92_729+93del	NP_115834.1:n.729+92_729+93del
NM_001015877.2:c.729+92_729+93del MANE Select	NP_001015877.1:n.729+92_729+93del
NM_032458.3:c.729+92_729+93del	NP_115834.1:n.729+92_729+93del