Canonical Allele Identifier: CA327518459

Gene: PHEX

Linked Data

• dbSNP Id: rs1005102138
• gnomAD v2: X-22065436-G-A
• gnomAD v3: X-22047318-G-A
• gnomAD v4: X-22047318-G-A
• MyVariant Identifiers: chrX:g.22065436G>A (hg19) ; chrX:g.22047318G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22047318G>A , CM000685.2:g.22047318G>A	GRCh38
NC_000023.10:g.22065436G>A , CM000685.1:g.22065436G>A	GRCh37
NC_000023.9:g.21975357G>A	NCBI36
NG_007563.2:g.19516G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.775+107G>A
ENST00000683214.1:n.544+14195G>A
ENST00000684143.1:c.349+107G>A	ENSP00000508264.1:n.349+107G>A
ENST00000379374.5:c.349+107G>A MANE Select	ENSP00000368682.4:n.349+107G>A
ENST00000379374.4:c.349+107G>A	ENSP00000368682.4:n.349+107G>A
NM_000444.5:c.349+107G>A	NP_000435.3:n.349+107G>A
NM_001282754.1:c.349+107G>A	NP_001269683.1:n.349+107G>A
XM_011545535.1:c.349+107G>A	XP_011543837.1:n.349+107G>A
XM_017029579.1:c.-94+107G>A	XP_016885068.1:n.-94+107G>A
XM_024452390.1:c.58+107G>A	XP_024308158.1:n.58+107G>A
XR_001755695.1:n.1028+107G>A
NM_000444.6:c.349+107G>A MANE Select	NP_000435.3:n.349+107G>A
NM_001282754.2:c.349+107G>A	NP_001269683.1:n.349+107G>A