Canonical Allele Identifier: CA1686656449

Gene: NXPH1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.8602762T= , CM000669.2:g.8602762T=	GRCh38
NC_000007.13:g.8642392T= , CM000669.1:g.8642392T=	GRCh37
NC_000007.12:g.8608917T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405863.6:c.55-148246T= MANE Select	ENSP00000384551.1:n.55-148246T=
ENST00000405863.5:c.55-148246T=	ENSP00000384551.1:n.55-148246T=
ENST00000429542.1:c.55-148246T=	ENSP00000408216.1:n.55-148246T=
ENST00000438764.1:c.55-148246T=	ENSP00000404689.1:n.55-148246T=
NM_152745.2:c.55-148246T=	NP_689958.1:n.55-148246T=
XR_927017.1:n.283-8327A=
XR_927018.1:n.312A=
XR_927019.1:n.283-8327A=
XR_927020.1:n.343-8327A=
XR_001745082.2:n.3273-8327A=
XR_001745083.2:n.573-8327A=
XR_001745084.1:n.3273-8327A=
XR_927017.3:n.3273-8327A=
XR_927019.2:n.3273-8327A=
NM_152745.3:c.55-148246T= MANE Select	NP_689958.1:n.55-148246T=