Canonical Allele Identifier: CA11021978
Gene: NPAS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100921242G>A , CM000664.2:g.100921242G>A GRCh38
NC_000002.11:g.101537704G>A , CM000664.1:g.101537704G>A GRCh37
NC_000002.10:g.100904136G>A NCBI36
NG_023259.1:g.106092G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000335681.10:c.33-3904G>A MANE Select ENSP00000338283.5:n.33-3904G>A
ENST00000335681.9:c.33-3904G>A ENSP00000338283.5:n.33-3904G>A
ENST00000427413.5:c.228-3904G>A ENSP00000397595.2:n.228-3904G>A
NM_002518.3:c.33-3904G>A NP_002509.2:n.33-3904G>A
XM_005263953.1:c.228-3904G>A XP_005264010.1:n.228-3904G>A
XM_005263954.1:c.228-3904G>A XP_005264011.1:n.228-3904G>A
XM_005263957.1:c.228-3904G>A XP_005264014.1:n.228-3904G>A
XM_005263959.1:c.228-3904G>A XP_005264016.1:n.228-3904G>A
XM_005263960.1:c.228-3904G>A XP_005264017.1:n.228-3904G>A
XM_011511242.1:c.33-3904G>A XP_011509544.1:n.33-3904G>A
XM_011511243.1:c.228-3904G>A XP_011509545.1:n.228-3904G>A
XR_922928.1:n.230-3904G>A
XM_005263953.2:c.228-3904G>A XP_005264010.1:n.228-3904G>A
XM_005263959.2:c.228-3904G>A XP_005264016.1:n.228-3904G>A
XM_005263960.2:c.228-3904G>A XP_005264017.1:n.228-3904G>A
XM_011511242.2:c.33-3904G>A XP_011509544.1:n.33-3904G>A
XM_011511243.2:c.228-3904G>A XP_011509545.1:n.228-3904G>A
XM_017004214.1:c.228-3904G>A XP_016859703.1:n.228-3904G>A
XM_017004215.1:c.228-3904G>A XP_016859704.1:n.228-3904G>A
XM_017004216.1:c.228-3904G>A XP_016859705.1:n.228-3904G>A
XM_017004217.1:c.228-3904G>A XP_016859706.1:n.228-3904G>A
NM_002518.4:c.33-3904G>A MANE Select NP_002509.2:n.33-3904G>A
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