Canonical Allele Identifier: CA11076362

Gene: NPAS2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100979013A>G , CM000664.2:g.100979013A>G	GRCh38
NC_000002.11:g.101595475A>G , CM000664.1:g.101595475A>G	GRCh37
NC_000002.10:g.100961907A>G	NCBI36
NG_023259.1:g.163863A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335681.10:c.1482+1214A>G MANE Select	ENSP00000338283.5:n.1482+1214A>G
ENST00000335681.9:c.1482+1214A>G	ENSP00000338283.5:n.1482+1214A>G
ENST00000450763.1:c.279+1214A>G	ENSP00000392125.1:n.279+1214A>G
ENST00000471974.1:n.342+1214A>G
ENST00000474550.5:n.816+1214A>G
NM_002518.3:c.1482+1214A>G	NP_002509.2:n.1482+1214A>G
XM_005263953.1:c.1677+1214A>G	XP_005264010.1:n.1677+1214A>G
XM_005263954.1:c.1677+1214A>G	XP_005264011.1:n.1677+1214A>G
XM_005263957.1:c.1563+1214A>G	XP_005264014.1:n.1563+1214A>G
XM_005263959.1:c.1677+1214A>G	XP_005264016.1:n.1677+1214A>G
XM_005263960.1:c.1368+1214A>G	XP_005264017.1:n.1368+1214A>G
XM_005263961.3:c.1110+1214A>G	XP_005264018.1:n.1110+1214A>G
XM_011511242.1:c.1392+1214A>G	XP_011509544.1:n.1392+1214A>G
XM_011511243.1:c.1677+1214A>G	XP_011509545.1:n.1677+1214A>G
XR_922928.1:n.1679+1214A>G
XM_005263953.2:c.1677+1214A>G	XP_005264010.1:n.1677+1214A>G
XM_005263959.2:c.1677+1214A>G	XP_005264016.1:n.1677+1214A>G
XM_005263960.2:c.1368+1214A>G	XP_005264017.1:n.1368+1214A>G
XM_005263961.4:c.1110+1214A>G	XP_005264018.1:n.1110+1214A>G
XM_011511242.2:c.1392+1214A>G	XP_011509544.1:n.1392+1214A>G
XM_011511243.2:c.1677+1214A>G	XP_011509545.1:n.1677+1214A>G
XM_017004214.1:c.1677+1214A>G	XP_016859703.1:n.1677+1214A>G
XM_017004215.1:c.1677+1214A>G	XP_016859704.1:n.1677+1214A>G
XM_017004216.1:c.1677+1214A>G	XP_016859705.1:n.1677+1214A>G
XM_017004217.1:c.1368+1214A>G	XP_016859706.1:n.1368+1214A>G
NM_002518.4:c.1482+1214A>G MANE Select	NP_002509.2:n.1482+1214A>G