Canonical Allele Identifier: CA1274583662

Gene: NPAS2 NPAS2-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100974842A= , CM000664.2:g.100974842A=	GRCh38
NC_000002.11:g.101591304A= , CM000664.1:g.101591304A=	GRCh37
NC_000002.10:g.100957736A=	NCBI36
NG_023259.1:g.159692A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335681.10:c.1180A= (NPAS2) MANE Select	ENSP00000338283.5:p.Thr394=
ENST00000335681.9:c.1180A= (NPAS2)	ENSP00000338283.5:p.Thr394=
ENST00000471974.1:n.40A= (NPAS2)
ENST00000474550.5:n.514A= (NPAS2)
NM_002518.3:c.1180A= (NPAS2)	NP_002509.2:p.Thr394=
NR_110213.1:n.575+443T= (NPAS2-AS1)
XM_005263953.1:c.1375A= (NPAS2)	XP_005264010.1:p.Thr459=
XM_005263954.1:c.1375A= (NPAS2)	XP_005264011.1:p.Thr459=
XM_005263957.1:c.1261A= (NPAS2)	XP_005264014.1:p.Thr421=
XM_005263959.1:c.1375A= (NPAS2)	XP_005264016.1:p.Thr459=
XM_005263960.1:c.1066A= (NPAS2)	XP_005264017.1:p.Thr356=
XM_005263961.3:c.808A= (NPAS2)	XP_005264018.1:p.Thr270=
XM_011511242.1:c.1090A= (NPAS2)	XP_011509544.1:p.Thr364=
XM_011511243.1:c.1375A= (NPAS2)	XP_011509545.1:p.Thr459=
XR_922928.1:n.1377A= (NPAS2)
XM_005263953.2:c.1375A= (NPAS2)	XP_005264010.1:p.Thr459=
XM_005263959.2:c.1375A= (NPAS2)	XP_005264016.1:p.Thr459=
XM_005263960.2:c.1066A= (NPAS2)	XP_005264017.1:p.Thr356=
XM_005263961.4:c.808A= (NPAS2)	XP_005264018.1:p.Thr270=
XM_011511242.2:c.1090A= (NPAS2)	XP_011509544.1:p.Thr364=
XM_011511243.2:c.1375A= (NPAS2)	XP_011509545.1:p.Thr459=
XM_017004214.1:c.1375A= (NPAS2)	XP_016859703.1:p.Thr459=
XM_017004215.1:c.1375A= (NPAS2)	XP_016859704.1:p.Thr459=
XM_017004216.1:c.1375A= (NPAS2)	XP_016859705.1:p.Thr459=
XM_017004217.1:c.1066A= (NPAS2)	XP_016859706.1:p.Thr356=
NM_002518.4:c.1180A= (NPAS2) MANE Select	NP_002509.2:p.Thr394=