Canonical Allele Identifier: CA2459717450
Gene: PHF6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.134413839A= , CM000685.2:g.134413839A= GRCh38
NC_000023.10:g.133547869A= , CM000685.1:g.133547869A= GRCh37
NC_000023.9:g.133375535A= NCBI36
NG_008886.1:g.45528A= , LRG_629:g.45528A=

Transcript Alleles

HGVS Amino-acid change
ENST00000685553.1:c.*521A= ENSP00000510193.1:n.*521A=
ENST00000687496.1:c.500A= ENSP00000509551.1:p.His167=
ENST00000688598.1:c.500A= ENSP00000510410.1:p.His167=
ENST00000691812.1:c.602A= ENSP00000510211.1:p.His201=
ENST00000693759.1:c.*214A= ENSP00000509518.1:n.*214A=
ENST00000370803.8:c.602A= MANE Select ENSP00000359839.4:p.His201=
ENST00000332070.7:c.602A= ENSP00000329097.3:p.His201=
ENST00000370799.5:c.605A= ENSP00000359835.1:p.His202=
ENST00000370800.4:c.605A= ENSP00000359836.4:p.His202=
ENST00000370803.7:c.602A= ENSP00000359839.3:p.His201=
ENST00000625464.2:c.605A= ENSP00000487420.1:p.His202=
NM_001015877.1:c.602A= , LRG_629t1:c.602A= NP_001015877.1:p.His201=
NM_032335.3:c.605A= , LRG_629t2:c.605A= NP_115711.2:p.His202=
NM_032458.2:c.602A= NP_115834.1:p.His201=
NM_001015877.2:c.602A= MANE Select NP_001015877.1:p.His201=
NM_032458.3:c.602A= NP_115834.1:p.His201=