Canonical Allele Identifier: CA414713077

Gene: PHF6

Linked Data

• MyVariant Identifiers: chrX:g.133547989A>T (hg19) ; chrX:g.134413959A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.134413959A>T , CM000685.2:g.134413959A>T	GRCh38
NC_000023.10:g.133547989A>T , CM000685.1:g.133547989A>T	GRCh37
NC_000023.9:g.133375655A>T	NCBI36
NG_008886.1:g.45648A>T , LRG_629:g.45648A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685553.1:c.*641A>T	ENSP00000510193.1:n.*641A>T
ENST00000687496.1:c.620A>T	ENSP00000509551.1:p.Lys207Met
ENST00000688598.1:c.620A>T	ENSP00000510410.1:p.Lys207Met
ENST00000691812.1:c.722A>T	ENSP00000510211.1:p.Lys241Met
ENST00000693759.1:c.*334A>T	ENSP00000509518.1:n.*334A>T
ENST00000370803.8:c.722A>T MANE Select	ENSP00000359839.4:p.Lys241Met
ENST00000332070.7:c.722A>T	ENSP00000329097.3:p.Lys241Met
ENST00000370799.5:c.725A>T	ENSP00000359835.1:p.Lys242Met
ENST00000370800.4:c.725A>T	ENSP00000359836.4:p.Lys242Met
ENST00000370803.7:c.722A>T	ENSP00000359839.3:p.Lys241Met
ENST00000625464.2:c.725A>T	ENSP00000487420.1:p.Lys242Met
NM_001015877.1:c.722A>T , LRG_629t1:c.722A>T	NP_001015877.1:p.Lys241Met
NM_032335.3:c.725A>T , LRG_629t2:c.725A>T	NP_115711.2:p.Lys242Met
NM_032458.2:c.722A>T	NP_115834.1:p.Lys241Met
NM_001015877.2:c.722A>T MANE Select	NP_001015877.1:p.Lys241Met
NM_032458.3:c.722A>T	NP_115834.1:p.Lys241Met