Canonical Allele Identifier: CA1274566104

Gene: NPAS2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100935633T>A , CM000664.2:g.100935633T>A	GRCh38
NC_000002.11:g.101552095T>A , CM000664.1:g.101552095T>A	GRCh37
NC_000002.10:g.100918527T>A	NCBI36
NG_023259.1:g.120483T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335681.10:c.274-2120T>A MANE Select	ENSP00000338283.5:n.274-2120T>A
ENST00000335681.9:c.274-2120T>A	ENSP00000338283.5:n.274-2120T>A
ENST00000427413.5:c.469-2120T>A	ENSP00000397595.2:n.469-2120T>A
ENST00000448812.5:c.242-2120T>A
ENST00000451740.1:c.232-2120T>A	ENSP00000395265.1:n.232-2120T>A
ENST00000486017.5:n.242-2120T>A
ENST00000492373.1:n.50+1473T>A
NM_002518.3:c.274-2120T>A	NP_002509.2:n.274-2120T>A
XM_005263953.1:c.469-2120T>A	XP_005264010.1:n.469-2120T>A
XM_005263954.1:c.469-2120T>A	XP_005264011.1:n.469-2120T>A
XM_005263957.1:c.469-2120T>A	XP_005264014.1:n.469-2120T>A
XM_005263959.1:c.469-2120T>A	XP_005264016.1:n.469-2120T>A
XM_005263960.1:c.469-2120T>A	XP_005264017.1:n.469-2120T>A
XM_005263961.3:c.-100+502T>A	XP_005264018.1:n.-100+502T>A
XM_011511242.1:c.273+2632T>A	XP_011509544.1:n.273+2632T>A
XM_011511243.1:c.469-2120T>A	XP_011509545.1:n.469-2120T>A
XR_922928.1:n.471-2120T>A
XM_005263953.2:c.469-2120T>A	XP_005264010.1:n.469-2120T>A
XM_005263959.2:c.469-2120T>A	XP_005264016.1:n.469-2120T>A
XM_005263960.2:c.469-2120T>A	XP_005264017.1:n.469-2120T>A
XM_005263961.4:c.-100+502T>A	XP_005264018.1:n.-100+502T>A
XM_011511242.2:c.273+2632T>A	XP_011509544.1:n.273+2632T>A
XM_011511243.2:c.469-2120T>A	XP_011509545.1:n.469-2120T>A
XM_017004214.1:c.469-2120T>A	XP_016859703.1:n.469-2120T>A
XM_017004215.1:c.469-2120T>A	XP_016859704.1:n.469-2120T>A
XM_017004216.1:c.469-2120T>A	XP_016859705.1:n.469-2120T>A
XM_017004217.1:c.469-2120T>A	XP_016859706.1:n.469-2120T>A
NM_002518.4:c.274-2120T>A MANE Select	NP_002509.2:n.274-2120T>A