Canonical Allele Identifier: CA1274589380

Gene: NPAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100987351T= , CM000664.2:g.100987351T=	GRCh38
NC_000002.11:g.101603813T= , CM000664.1:g.101603813T=	GRCh37
NC_000002.10:g.100970245T=	NCBI36
NG_023259.1:g.172201T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000335681.10:c.1630-728T= MANE Select	ENSP00000338283.5:n.1630-728T=
ENST00000335681.9:c.1630-728T=	ENSP00000338283.5:n.1630-728T=
ENST00000433408.1:c.125-728T=
ENST00000450763.1:c.426+4974T=	ENSP00000392125.1:n.426+4974T=
ENST00000474550.5:n.5937T=
NM_002518.3:c.1630-728T=	NP_002509.2:n.1630-728T=
XM_005263953.1:c.1825-728T=	XP_005264010.1:n.1825-728T=
XM_005263954.1:c.1825-728T=	XP_005264011.1:n.1825-728T=
XM_005263957.1:c.1711-728T=	XP_005264014.1:n.1711-728T=
XM_005263959.1:c.1825-728T=	XP_005264016.1:n.1825-728T=
XM_005263960.1:c.1516-728T=	XP_005264017.1:n.1516-728T=
XM_005263961.3:c.1258-728T=	XP_005264018.1:n.1258-728T=
XM_011511242.1:c.1540-728T=	XP_011509544.1:n.1540-728T=
XR_922928.1:n.1827-728T=
XM_005263953.2:c.1825-728T=	XP_005264010.1:n.1825-728T=
XM_005263959.2:c.1825-728T=	XP_005264016.1:n.1825-728T=
XM_005263960.2:c.1516-728T=	XP_005264017.1:n.1516-728T=
XM_005263961.4:c.1258-728T=	XP_005264018.1:n.1258-728T=
XM_011511242.2:c.1540-728T=	XP_011509544.1:n.1540-728T=
XM_017004214.1:c.1825-728T=	XP_016859703.1:n.1825-728T=
XM_017004215.1:c.1825-728T=	XP_016859704.1:n.1825-728T=
XM_017004216.1:c.1825-728T=	XP_016859705.1:n.1825-728T=
XM_017004217.1:c.1516-728T=	XP_016859706.1:n.1516-728T=
NM_002518.4:c.1630-728T= MANE Select	NP_002509.2:n.1630-728T=