Canonical Allele Identifier: CA1686656418

Gene: NXPH1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.8602742G= , CM000669.2:g.8602742G=	GRCh38
NC_000007.13:g.8642372G= , CM000669.1:g.8642372G=	GRCh37
NC_000007.12:g.8608897G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405863.6:c.55-148266G= MANE Select	ENSP00000384551.1:n.55-148266G=
ENST00000405863.5:c.55-148266G=	ENSP00000384551.1:n.55-148266G=
ENST00000429542.1:c.55-148266G=	ENSP00000408216.1:n.55-148266G=
ENST00000438764.1:c.55-148266G=	ENSP00000404689.1:n.55-148266G=
NM_152745.2:c.55-148266G=	NP_689958.1:n.55-148266G=
XR_927017.1:n.283-8307C=
XR_927018.1:n.332C=
XR_927019.1:n.283-8307C=
XR_927020.1:n.343-8307C=
XR_001745082.2:n.3273-8307C=
XR_001745083.2:n.573-8307C=
XR_001745084.1:n.3273-8307C=
XR_927017.3:n.3273-8307C=
XR_927019.2:n.3273-8307C=
NM_152745.3:c.55-148266G= MANE Select	NP_689958.1:n.55-148266G=