Canonical Allele Identifier: CA259120075
Gene: NPAS3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.33117357G>A , CM000676.2:g.33117357G>A GRCh38
NC_000014.8:g.33586563G>A , CM000676.1:g.33586563G>A GRCh37
NC_000014.7:g.32656314G>A NCBI36
NG_013036.1:g.183105G>A
NG_013036.2:g.183105G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356141.9:c.140+61363G>A MANE Select ENSP00000348460.4:n.140+61363G>A
ENST00000551634.6:c.159-97825G>A ENSP00000448373.2:n.159-97825G>A
ENST00000346562.6:c.51-97825G>A ENSP00000319610.5:n.51-97825G>A
ENST00000356141.8:c.140+61363G>A ENSP00000348460.4:n.140+61363G>A
ENST00000357798.9:c.51-97825G>A ENSP00000350446.5:n.51-97825G>A
ENST00000548645.5:c.51-97825G>A ENSP00000448916.1:n.51-97825G>A
ENST00000551492.5:c.161+61363G>A ENSP00000450392.1:n.161+61363G>A
ENST00000551634.5:c.72-97825G>A ENSP00000448373.1:n.72-97825G>A
NM_001164749.1:c.140+61363G>A NP_001158221.1:n.140+61363G>A
NM_001165893.1:c.51-97825G>A NP_001159365.1:n.51-97825G>A
NM_022123.2:c.51-97825G>A NP_071406.1:n.51-97825G>A
NM_173159.2:c.51-97825G>A NP_775182.1:n.51-97825G>A
XM_005267991.2:c.161+61363G>A XP_005268048.1:n.161+61363G>A
XM_005267992.2:c.161+61363G>A XP_005268049.1:n.161+61363G>A
XM_005267993.2:c.50+61347G>A XP_005268050.1:n.50+61347G>A
XM_011537067.1:c.140+61363G>A XP_011535369.1:n.140+61363G>A
XM_011537068.1:c.140+61363G>A XP_011535370.1:n.140+61363G>A
XM_011537069.1:c.161+61363G>A XP_011535371.1:n.161+61363G>A
XM_011537070.1:c.51-97825G>A XP_011535372.1:n.51-97825G>A
XM_011537071.1:c.72-97825G>A XP_011535373.1:n.72-97825G>A
XM_011537072.1:c.51-97825G>A XP_011535374.1:n.51-97825G>A
XM_005267991.3:c.248+61363G>A XP_005268048.2:n.248+61363G>A
XM_005267992.3:c.248+61363G>A XP_005268049.2:n.248+61363G>A
XM_011537067.2:c.140+61363G>A XP_011535369.1:n.140+61363G>A
XM_011537069.2:c.248+61363G>A XP_011535371.2:n.248+61363G>A
XM_011537070.2:c.51-97825G>A XP_011535372.1:n.51-97825G>A
XM_011537071.2:c.159-97825G>A XP_011535373.2:n.159-97825G>A
XM_011537072.2:c.51-97825G>A XP_011535374.1:n.51-97825G>A
XM_017021582.1:c.248+61363G>A XP_016877071.1:n.248+61363G>A
XM_017021583.1:c.248+61363G>A XP_016877072.1:n.248+61363G>A
XM_017021584.1:c.159-97825G>A XP_016877073.1:n.159-97825G>A
XM_017021585.1:c.159-97825G>A XP_016877074.1:n.159-97825G>A
XM_017021586.1:c.-220G>A XP_016877075.1:n.-220G>A
NM_001164749.2:c.140+61363G>A MANE Select NP_001158221.1:n.140+61363G>A
NM_001165893.2:c.51-97825G>A NP_001159365.1:n.51-97825G>A
NM_022123.3:c.51-97825G>A NP_071406.1:n.51-97825G>A
NM_173159.3:c.51-97825G>A NP_775182.1:n.51-97825G>A
NM_001394988.1:c.51-97825G>A NP_001381917.1:n.51-97825G>A
NM_001394989.1:c.51-97825G>A NP_001381918.1:n.51-97825G>A
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