Canonical Allele Identifier: CA2419168529

Gene: PHEX

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.22096819_22096820delinsTC , CM000685.2:g.22096819_22096820delinsTC	GRCh38
NC_000023.10:g.22114937_22114938delinsTC , CM000685.1:g.22114937_22114938delinsTC	GRCh37
NC_000023.9:g.22024858_22024859delinsTC	NCBI36
NG_007563.2:g.69017_69018delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000475778.2:n.1276-136_1276-135delinsTC
ENST00000684143.1:c.847-136_847-135delinsTC	ENSP00000508264.1:n.847-136_847-135delinsTC
ENST00000684745.1:n.524-136_524-135delinsTC
ENST00000379374.5:c.850-136_850-135delinsTC MANE Select	ENSP00000368682.4:n.850-136_850-135delinsTC
ENST00000379374.4:c.850-136_850-135delinsTC	ENSP00000368682.4:n.850-136_850-135delinsTC
ENST00000475778.1:n.123-136_123-135delinsTC
NM_000444.5:c.850-136_850-135delinsTC	NP_000435.3:n.850-136_850-135delinsTC
NM_001282754.1:c.850-136_850-135delinsTC	NP_001269683.1:n.850-136_850-135delinsTC
XM_011545533.1:c.94-136_94-135delinsTC	XP_011543835.1:n.94-136_94-135delinsTC
XM_011545534.1:c.94-136_94-135delinsTC	XP_011543836.1:n.94-136_94-135delinsTC
XM_011545535.1:c.850-136_850-135delinsTC	XP_011543837.1:n.850-136_850-135delinsTC
XM_017029579.1:c.94-136_94-135delinsTC	XP_016885068.1:n.94-136_94-135delinsTC
XM_024452390.1:c.559-136_559-135delinsTC	XP_024308158.1:n.559-136_559-135delinsTC
XR_001755695.1:n.1529-136_1529-135delinsTC
NM_000444.6:c.850-136_850-135delinsTC MANE Select	NP_000435.3:n.850-136_850-135delinsTC
NM_001282754.2:c.850-136_850-135delinsTC	NP_001269683.1:n.850-136_850-135delinsTC