Canonical Allele Identifier: CA389412944

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269392G>A (hg19) ; chr14:g.33800186G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800186G>A , CM000676.2:g.33800186G>A	GRCh38
NC_000014.8:g.34269392G>A , CM000676.1:g.34269392G>A	GRCh37
NC_000014.7:g.33339143G>A	NCBI36
NG_013036.1:g.865934G>A
NG_013036.2:g.865934G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1879G>A MANE Select	ENSP00000348460.4:p.Asp627Asn
ENST00000551634.6:c.1888G>A	ENSP00000448373.2:p.Asp630Asn
ENST00000680362.1:c.1779G>A
ENST00000681323.1:c.793+2605G>A
ENST00000346562.6:c.1783G>A	ENSP00000319610.5:p.Asp595Asn
ENST00000356141.8:c.1879G>A	ENSP00000348460.4:p.Asp627Asn
ENST00000357798.9:c.1840G>A	ENSP00000350446.5:p.Asp614Asn
ENST00000548645.5:c.1789G>A	ENSP00000448916.1:p.Asp597Asn
ENST00000551492.5:c.1894G>A	ENSP00000450392.1:p.Asp632Asn
ENST00000551634.5:c.1801G>A	ENSP00000448373.1:p.Asp601Asn
NM_001164749.1:c.1879G>A	NP_001158221.1:p.Asp627Asn
NM_001165893.1:c.1789G>A	NP_001159365.1:p.Asp597Asn
NM_022123.2:c.1783G>A	NP_071406.1:p.Asp595Asn
NM_173159.2:c.1840G>A	NP_775182.1:p.Asp614Asn
XM_005267991.2:c.1900G>A	XP_005268048.1:p.Asp634Asn
XM_005267992.2:c.1894G>A	XP_005268049.1:p.Asp632Asn
XM_005267993.2:c.1840G>A	XP_005268050.1:p.Asp614Asn
XM_011537067.1:c.1930G>A	XP_011535369.1:p.Asp644Asn
XM_011537068.1:c.1921G>A	XP_011535370.1:p.Asp641Asn
XM_011537069.1:c.1891G>A	XP_011535371.1:p.Asp631Asn
XM_011537070.1:c.1834G>A	XP_011535372.1:p.Asp612Asn
XM_011537071.1:c.1801G>A	XP_011535373.1:p.Asp601Asn
XM_011537072.1:c.1780G>A	XP_011535374.1:p.Asp594Asn
XM_011537073.1:c.1573G>A	XP_011535375.1:p.Asp525Asn
XM_011537074.1:c.1573G>A	XP_011535376.1:p.Asp525Asn
XM_005267991.3:c.1987G>A	XP_005268048.2:p.Asp663Asn
XM_005267992.3:c.1981G>A	XP_005268049.2:p.Asp661Asn
XM_011537067.2:c.1930G>A	XP_011535369.1:p.Asp644Asn
XM_011537069.2:c.1978G>A	XP_011535371.2:p.Asp660Asn
XM_011537070.2:c.1834G>A	XP_011535372.1:p.Asp612Asn
XM_011537071.2:c.1888G>A	XP_011535373.2:p.Asp630Asn
XM_011537072.2:c.1780G>A	XP_011535374.1:p.Asp594Asn
XM_017021582.1:c.2038G>A	XP_016877071.1:p.Asp680Asn
XM_017021583.1:c.2029G>A	XP_016877072.1:p.Asp677Asn
XM_017021584.1:c.1948G>A	XP_016877073.1:p.Asp650Asn
XM_017021585.1:c.1897G>A	XP_016877074.1:p.Asp633Asn
XM_017021586.1:c.1573G>A	XP_016877075.1:p.Asp525Asn
XM_017021587.1:c.1573G>A	XP_016877076.1:p.Asp525Asn
XM_017021588.1:c.1573G>A	XP_016877077.1:p.Asp525Asn
NM_001164749.2:c.1879G>A MANE Select	NP_001158221.1:p.Asp627Asn
NM_001165893.2:c.1789G>A	NP_001159365.1:p.Asp597Asn
NM_022123.3:c.1783G>A	NP_071406.1:p.Asp595Asn
NM_173159.3:c.1840G>A	NP_775182.1:p.Asp614Asn
NM_001394988.1:c.1834G>A	NP_001381917.1:p.Asp612Asn
NM_001394989.1:c.1780G>A	NP_001381918.1:p.Asp594Asn