Canonical Allele Identifier: CA1274534003

Gene: NPAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100862577C= , CM000664.2:g.100862577C=	GRCh38
NC_000002.11:g.101479039C= , CM000664.1:g.101479039C=	GRCh37
NC_000002.10:g.100845471C=	NCBI36
NG_023259.1:g.47427C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000335681.10:c.-22-42156C= MANE Select	ENSP00000338283.5:n.-22-42156C=
ENST00000335681.9:c.-22-42156C=	ENSP00000338283.5:n.-22-42156C=
ENST00000427413.5:c.173+41378C=	ENSP00000397595.2:n.173+41378C=
NM_002518.3:c.-22-42156C=	NP_002509.2:n.-22-42156C=
XM_005263953.1:c.173+41378C=	XP_005264010.1:n.173+41378C=
XM_005263954.1:c.173+41378C=	XP_005264011.1:n.173+41378C=
XM_005263957.1:c.173+41378C=	XP_005264014.1:n.173+41378C=
XM_005263959.1:c.173+41378C=	XP_005264016.1:n.173+41378C=
XM_005263960.1:c.173+41378C=	XP_005264017.1:n.173+41378C=
XM_011511242.1:c.-22-42156C=	XP_011509544.1:n.-22-42156C=
XM_011511243.1:c.173+41378C=	XP_011509545.1:n.173+41378C=
XR_922928.1:n.175+41378C=
XM_005263953.2:c.173+41378C=	XP_005264010.1:n.173+41378C=
XM_005263959.2:c.173+41378C=	XP_005264016.1:n.173+41378C=
XM_005263960.2:c.173+41378C=	XP_005264017.1:n.173+41378C=
XM_011511242.2:c.-22-42156C=	XP_011509544.1:n.-22-42156C=
XM_011511243.2:c.173+41378C=	XP_011509545.1:n.173+41378C=
XM_017004214.1:c.173+41378C=	XP_016859703.1:n.173+41378C=
XM_017004215.1:c.173+41378C=	XP_016859704.1:n.173+41378C=
XM_017004216.1:c.173+41378C=	XP_016859705.1:n.173+41378C=
XM_017004217.1:c.173+41378C=	XP_016859706.1:n.173+41378C=
NM_002518.4:c.-22-42156C= MANE Select	NP_002509.2:n.-22-42156C=