Canonical Allele Identifier: CA2693304878

Gene: PHEX

Linked Data

• gnomAD v4: X-22096944-CTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096947_22096948del , CM000685.2:g.22096947_22096948del	GRCh38
NC_000023.10:g.22115065_22115066del , CM000685.1:g.22115065_22115066del	GRCh37
NC_000023.9:g.22024986_22024987del	NCBI36
NG_007563.2:g.69145_69146del

Transcript Alleles

HGVS	Amino-acid change
ENST00000475778.2:n.1276-8_1276-7del
ENST00000684143.1:c.847-8_847-7del	ENSP00000508264.1:n.847-8_847-7del
ENST00000684745.1:n.524-8_524-7del
ENST00000379374.5:c.850-8_850-7del MANE Select	ENSP00000368682.4:n.850-8_850-7del
ENST00000379374.4:c.850-8_850-7del	ENSP00000368682.4:n.850-8_850-7del
ENST00000475778.1:n.123-8_123-7del
NM_000444.5:c.850-8_850-7del	NP_000435.3:n.850-8_850-7del
NM_001282754.1:c.850-8_850-7del	NP_001269683.1:n.850-8_850-7del
XM_011545533.1:c.94-8_94-7del	XP_011543835.1:n.94-8_94-7del
XM_011545534.1:c.94-8_94-7del	XP_011543836.1:n.94-8_94-7del
XM_011545535.1:c.850-8_850-7del	XP_011543837.1:n.850-8_850-7del
XM_017029579.1:c.94-8_94-7del	XP_016885068.1:n.94-8_94-7del
XM_024452390.1:c.559-8_559-7del	XP_024308158.1:n.559-8_559-7del
XR_001755695.1:n.1529-8_1529-7del
NM_000444.6:c.850-8_850-7del MANE Select	NP_000435.3:n.850-8_850-7del
NM_001282754.2:c.850-8_850-7del	NP_001269683.1:n.850-8_850-7del