Canonical Allele Identifier: CA1274526675

Gene: NPAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100843539_100843540delinsGT , CM000664.2:g.100843539_100843540delinsGT	GRCh38
NC_000002.11:g.101460001_101460002delinsGT , CM000664.1:g.101460001_101460002delinsGT	GRCh37
NC_000002.10:g.100826433_100826434delinsGT	NCBI36
NG_023259.1:g.28389_28390delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000335681.10:c.-23+23125_-23+23126delinsGT MANE Select	ENSP00000338283.5:n.-23+23125_-23+23126de...
ENST00000335681.9:c.-23+23125_-23+23126delinsGT	ENSP00000338283.5:n.-23+23125_-23+23126de...
ENST00000427413.5:c.173+22340_173+22341delinsGT	ENSP00000397595.2:n.173+22340_173+22341de...
NM_002518.3:c.-23+23125_-23+23126delinsGT	NP_002509.2:n.-23+23125_-23+23126delinsGT...
XM_005263953.1:c.173+22340_173+22341delinsGT	XP_005264010.1:n.173+22340_173+22341delin...
XM_005263954.1:c.173+22340_173+22341delinsGT	XP_005264011.1:n.173+22340_173+22341delin...
XM_005263957.1:c.173+22340_173+22341delinsGT	XP_005264014.1:n.173+22340_173+22341delin...
XM_005263959.1:c.173+22340_173+22341delinsGT	XP_005264016.1:n.173+22340_173+22341delin...
XM_005263960.1:c.173+22340_173+22341delinsGT	XP_005264017.1:n.173+22340_173+22341delin...
XM_011511242.1:c.-23+23125_-23+23126delinsGT	XP_011509544.1:n.-23+23125_-23+23126delin...
XM_011511243.1:c.173+22340_173+22341delinsGT	XP_011509545.1:n.173+22340_173+22341delin...
XR_922928.1:n.175+22340_175+22341delinsGT
XM_005263953.2:c.173+22340_173+22341delinsGT	XP_005264010.1:n.173+22340_173+22341delin...
XM_005263959.2:c.173+22340_173+22341delinsGT	XP_005264016.1:n.173+22340_173+22341delin...
XM_005263960.2:c.173+22340_173+22341delinsGT	XP_005264017.1:n.173+22340_173+22341delin...
XM_011511242.2:c.-23+23125_-23+23126delinsGT	XP_011509544.1:n.-23+23125_-23+23126delin...
XM_011511243.2:c.173+22340_173+22341delinsGT	XP_011509545.1:n.173+22340_173+22341delin...
XM_017004214.1:c.173+22340_173+22341delinsGT	XP_016859703.1:n.173+22340_173+22341delin...
XM_017004215.1:c.173+22340_173+22341delinsGT	XP_016859704.1:n.173+22340_173+22341delin...
XM_017004216.1:c.173+22340_173+22341delinsGT	XP_016859705.1:n.173+22340_173+22341delin...
XM_017004217.1:c.173+22340_173+22341delinsGT	XP_016859706.1:n.173+22340_173+22341delin...
NM_002518.4:c.-23+23125_-23+23126delinsGT MANE Select	NP_002509.2:n.-23+23125_-23+23126delinsGT...