Canonical Allele Identifier: CA1274534002

Gene: NPAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.100862575_100862576delinsGC , CM000664.2:g.100862575_100862576delinsGC	GRCh38
NC_000002.11:g.101479037_101479038delinsGC , CM000664.1:g.101479037_101479038delinsGC	GRCh37
NC_000002.10:g.100845469_100845470delinsGC	NCBI36
NG_023259.1:g.47425_47426delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335681.10:c.-22-42158_-22-42157delinsGC MANE Select	ENSP00000338283.5:n.-22-42158_-22-42157delinsGC
ENST00000335681.9:c.-22-42158_-22-42157delinsGC	ENSP00000338283.5:n.-22-42158_-22-42157delinsGC
ENST00000427413.5:c.173+41376_173+41377delinsGC	ENSP00000397595.2:n.173+41376_173+41377delinsGC
NM_002518.3:c.-22-42158_-22-42157delinsGC	NP_002509.2:n.-22-42158_-22-42157delinsGC
XM_005263953.1:c.173+41376_173+41377delinsGC	XP_005264010.1:n.173+41376_173+41377delinsGC
XM_005263954.1:c.173+41376_173+41377delinsGC	XP_005264011.1:n.173+41376_173+41377delinsGC
XM_005263957.1:c.173+41376_173+41377delinsGC	XP_005264014.1:n.173+41376_173+41377delinsGC
XM_005263959.1:c.173+41376_173+41377delinsGC	XP_005264016.1:n.173+41376_173+41377delinsGC
XM_005263960.1:c.173+41376_173+41377delinsGC	XP_005264017.1:n.173+41376_173+41377delinsGC
XM_011511242.1:c.-22-42158_-22-42157delinsGC	XP_011509544.1:n.-22-42158_-22-42157delinsGC
XM_011511243.1:c.173+41376_173+41377delinsGC	XP_011509545.1:n.173+41376_173+41377delinsGC
XR_922928.1:n.175+41376_175+41377delinsGC
XM_005263953.2:c.173+41376_173+41377delinsGC	XP_005264010.1:n.173+41376_173+41377delinsGC
XM_005263959.2:c.173+41376_173+41377delinsGC	XP_005264016.1:n.173+41376_173+41377delinsGC
XM_005263960.2:c.173+41376_173+41377delinsGC	XP_005264017.1:n.173+41376_173+41377delinsGC
XM_011511242.2:c.-22-42158_-22-42157delinsGC	XP_011509544.1:n.-22-42158_-22-42157delinsGC
XM_011511243.2:c.173+41376_173+41377delinsGC	XP_011509545.1:n.173+41376_173+41377delinsGC
XM_017004214.1:c.173+41376_173+41377delinsGC	XP_016859703.1:n.173+41376_173+41377delinsGC
XM_017004215.1:c.173+41376_173+41377delinsGC	XP_016859704.1:n.173+41376_173+41377delinsGC
XM_017004216.1:c.173+41376_173+41377delinsGC	XP_016859705.1:n.173+41376_173+41377delinsGC
XM_017004217.1:c.173+41376_173+41377delinsGC	XP_016859706.1:n.173+41376_173+41377delinsGC
NM_002518.4:c.-22-42158_-22-42157delinsGC MANE Select	NP_002509.2:n.-22-42158_-22-42157delinsGC