Canonical Allele Identifier: CA389414324

Gene: NPAS3

Linked Data

• gnomAD v4: 14-33800576-G-A
• MyVariant Identifiers: chr14:g.34269782G>A (hg19) ; chr14:g.33800576G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800576G>A , CM000676.2:g.33800576G>A	GRCh38
NC_000014.8:g.34269782G>A , CM000676.1:g.34269782G>A	GRCh37
NC_000014.7:g.33339533G>A	NCBI36
NG_013036.1:g.866324G>A
NG_013036.2:g.866324G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2269G>A MANE Select	ENSP00000348460.4:p.Asp757Asn
ENST00000551634.6:c.2278G>A	ENSP00000448373.2:p.Asp760Asn
ENST00000680362.1:c.2169G>A
ENST00000681323.1:c.793+2995G>A
ENST00000346562.6:c.2173G>A	ENSP00000319610.5:p.Asp725Asn
ENST00000356141.8:c.2269G>A	ENSP00000348460.4:p.Asp757Asn
ENST00000357798.9:c.2230G>A	ENSP00000350446.5:p.Asp744Asn
ENST00000548645.5:c.2179G>A	ENSP00000448916.1:p.Asp727Asn
ENST00000551492.5:c.2284G>A	ENSP00000450392.1:p.Asp762Asn
ENST00000551634.5:c.2191G>A	ENSP00000448373.1:p.Asp731Asn
NM_001164749.1:c.2269G>A	NP_001158221.1:p.Asp757Asn
NM_001165893.1:c.2179G>A	NP_001159365.1:p.Asp727Asn
NM_022123.2:c.2173G>A	NP_071406.1:p.Asp725Asn
NM_173159.2:c.2230G>A	NP_775182.1:p.Asp744Asn
XM_005267991.2:c.2290G>A	XP_005268048.1:p.Asp764Asn
XM_005267992.2:c.2284G>A	XP_005268049.1:p.Asp762Asn
XM_005267993.2:c.2230G>A	XP_005268050.1:p.Asp744Asn
XM_011537067.1:c.2320G>A	XP_011535369.1:p.Asp774Asn
XM_011537068.1:c.2311G>A	XP_011535370.1:p.Asp771Asn
XM_011537069.1:c.2281G>A	XP_011535371.1:p.Asp761Asn
XM_011537070.1:c.2224G>A	XP_011535372.1:p.Asp742Asn
XM_011537071.1:c.2191G>A	XP_011535373.1:p.Asp731Asn
XM_011537072.1:c.2170G>A	XP_011535374.1:p.Asp724Asn
XM_011537073.1:c.1963G>A	XP_011535375.1:p.Asp655Asn
XM_011537074.1:c.1963G>A	XP_011535376.1:p.Asp655Asn
XM_005267991.3:c.2377G>A	XP_005268048.2:p.Asp793Asn
XM_005267992.3:c.2371G>A	XP_005268049.2:p.Asp791Asn
XM_011537067.2:c.2320G>A	XP_011535369.1:p.Asp774Asn
XM_011537069.2:c.2368G>A	XP_011535371.2:p.Asp790Asn
XM_011537070.2:c.2224G>A	XP_011535372.1:p.Asp742Asn
XM_011537071.2:c.2278G>A	XP_011535373.2:p.Asp760Asn
XM_011537072.2:c.2170G>A	XP_011535374.1:p.Asp724Asn
XM_017021582.1:c.2428G>A	XP_016877071.1:p.Asp810Asn
XM_017021583.1:c.2419G>A	XP_016877072.1:p.Asp807Asn
XM_017021584.1:c.2338G>A	XP_016877073.1:p.Asp780Asn
XM_017021585.1:c.2287G>A	XP_016877074.1:p.Asp763Asn
XM_017021586.1:c.1963G>A	XP_016877075.1:p.Asp655Asn
XM_017021587.1:c.1963G>A	XP_016877076.1:p.Asp655Asn
XM_017021588.1:c.1963G>A	XP_016877077.1:p.Asp655Asn
NM_001164749.2:c.2269G>A MANE Select	NP_001158221.1:p.Asp757Asn
NM_001165893.2:c.2179G>A	NP_001159365.1:p.Asp727Asn
NM_022123.3:c.2173G>A	NP_071406.1:p.Asp725Asn
NM_173159.3:c.2230G>A	NP_775182.1:p.Asp744Asn
NM_001394988.1:c.2224G>A	NP_001381917.1:p.Asp742Asn
NM_001394989.1:c.2170G>A	NP_001381918.1:p.Asp724Asn