Canonical Allele Identifier: CA1274568683

Gene: NPAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100941104G= , CM000664.2:g.100941104G=	GRCh38
NC_000002.11:g.101557566G= , CM000664.1:g.101557566G=	GRCh37
NC_000002.10:g.100923998G=	NCBI36
NG_023259.1:g.125954G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335681.10:c.363+3262G= MANE Select	ENSP00000338283.5:n.363+3262G=
ENST00000335681.9:c.363+3262G=	ENSP00000338283.5:n.363+3262G=
ENST00000427413.5:c.558+3262G=	ENSP00000397595.2:n.558+3262G=
ENST00000448812.5:c.331+3262G=
ENST00000486017.5:n.331+3262G=
ENST00000492373.1:n.140+3262G=
NM_002518.3:c.363+3262G=	NP_002509.2:n.363+3262G=
XM_005263953.1:c.558+3262G=	XP_005264010.1:n.558+3262G=
XM_005263954.1:c.558+3262G=	XP_005264011.1:n.558+3262G=
XM_005263957.1:c.558+3262G=	XP_005264014.1:n.558+3262G=
XM_005263959.1:c.558+3262G=	XP_005264016.1:n.558+3262G=
XM_005263960.1:c.558+3262G=	XP_005264017.1:n.558+3262G=
XM_005263961.3:c.-10+3262G=	XP_005264018.1:n.-10+3262G=
XM_011511242.1:c.274-7131G=	XP_011509544.1:n.274-7131G=
XM_011511243.1:c.558+3262G=	XP_011509545.1:n.558+3262G=
XR_922928.1:n.560+3262G=
XM_005263953.2:c.558+3262G=	XP_005264010.1:n.558+3262G=
XM_005263959.2:c.558+3262G=	XP_005264016.1:n.558+3262G=
XM_005263960.2:c.558+3262G=	XP_005264017.1:n.558+3262G=
XM_005263961.4:c.-10+3262G=	XP_005264018.1:n.-10+3262G=
XM_011511242.2:c.274-7131G=	XP_011509544.1:n.274-7131G=
XM_011511243.2:c.558+3262G=	XP_011509545.1:n.558+3262G=
XM_017004214.1:c.558+3262G=	XP_016859703.1:n.558+3262G=
XM_017004215.1:c.558+3262G=	XP_016859704.1:n.558+3262G=
XM_017004216.1:c.558+3262G=	XP_016859705.1:n.558+3262G=
XM_017004217.1:c.558+3262G=	XP_016859706.1:n.558+3262G=
NM_002518.4:c.363+3262G= MANE Select	NP_002509.2:n.363+3262G=