Canonical Allele Identifier: CA2693831586

Gene: PHF8

Linked Data

• gnomAD v4: X-54043206-CAGCGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.54043207_54043211del , CM000685.2:g.54043207_54043211del	GRCh38
NC_000023.10:g.54069640_54069644del , CM000685.1:g.54069640_54069644del	GRCh37
NC_000023.9:g.54086365_54086369del	NCBI36
NG_021309.1:g.6926_6930del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686349.1:c.-92-391_-92-387del	ENSP00000510424.1:n.-92-391_-92-387del
ENST00000687764.1:c.-92-391_-92-387del	ENSP00000509967.1:n.-92-391_-92-387del
ENST00000338154.11:c.-92-391_-92-387del MANE Select	ENSP00000338868.6:n.-92-391_-92-387del
ENST00000338154.10:c.-92-391_-92-387del	ENSP00000338868.6:n.-92-391_-92-387del
ENST00000338946.10:c.-92-391_-92-387del	ENSP00000340051.6:n.-92-391_-92-387del
ENST00000357988.9:c.17-391_17-387del	ENSP00000350676.5:n.17-391_17-387del
ENST00000415025.5:c.-92-391_-92-387del	ENSP00000404117.1:n.-92-391_-92-387del
ENST00000437224.5:c.-81-402_-81-398del	ENSP00000398995.1:n.-81-402_-81-398del
ENST00000453905.5:c.17-391_17-387del	ENSP00000405897.1:n.17-391_17-387del
NM_001184896.1:c.17-391_17-387del	NP_001171825.1:n.17-391_17-387del
NM_001184897.1:c.-92-391_-92-387del	NP_001171826.1:n.-92-391_-92-387del
NM_015107.2:c.-92-391_-92-387del	NP_055922.1:n.-92-391_-92-387del
XM_005261996.1:c.17-391_17-387del	XP_005262053.1:n.17-391_17-387del
XM_005261997.2:c.-92-391_-92-387del	XP_005262054.1:n.-92-391_-92-387del
XM_005262000.1:c.17-391_17-387del	XP_005262057.1:n.17-391_17-387del
XM_006724585.1:c.17-391_17-387del	XP_006724648.1:n.17-391_17-387del
XM_011530778.1:c.17-391_17-387del	XP_011529080.1:n.17-391_17-387del
XM_005261997.4:c.-92-391_-92-387del	XP_005262054.1:n.-92-391_-92-387del
XM_017029361.2:c.-92-391_-92-387del	XP_016884850.1:n.-92-391_-92-387del
XM_017029362.2:c.-92-391_-92-387del	XP_016884851.1:n.-92-391_-92-387del
NM_015107.3:c.-92-391_-92-387del MANE Select	NP_055922.1:n.-92-391_-92-387del
NM_001184897.2:c.-92-391_-92-387del	NP_001171826.1:n.-92-391_-92-387del