Canonical Allele Identifier: CA389412947

Gene: NPAS3

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1879G>T MANE Select	ENSP00000348460.4:p.Asp627Tyr
ENST00000551634.6:c.1888G>T	ENSP00000448373.2:p.Asp630Tyr
ENST00000680362.1:c.1779G>T
ENST00000681323.1:c.793+2605G>T
ENST00000346562.6:c.1783G>T	ENSP00000319610.5:p.Asp595Tyr
ENST00000356141.8:c.1879G>T	ENSP00000348460.4:p.Asp627Tyr
ENST00000357798.9:c.1840G>T	ENSP00000350446.5:p.Asp614Tyr
ENST00000548645.5:c.1789G>T	ENSP00000448916.1:p.Asp597Tyr
ENST00000551492.5:c.1894G>T	ENSP00000450392.1:p.Asp632Tyr
ENST00000551634.5:c.1801G>T	ENSP00000448373.1:p.Asp601Tyr
NM_001164749.1:c.1879G>T	NP_001158221.1:p.Asp627Tyr
NM_001165893.1:c.1789G>T	NP_001159365.1:p.Asp597Tyr
NM_022123.2:c.1783G>T	NP_071406.1:p.Asp595Tyr
NM_173159.2:c.1840G>T	NP_775182.1:p.Asp614Tyr
XM_005267991.2:c.1900G>T	XP_005268048.1:p.Asp634Tyr
XM_005267992.2:c.1894G>T	XP_005268049.1:p.Asp632Tyr
XM_005267993.2:c.1840G>T	XP_005268050.1:p.Asp614Tyr
XM_011537067.1:c.1930G>T	XP_011535369.1:p.Asp644Tyr
XM_011537068.1:c.1921G>T	XP_011535370.1:p.Asp641Tyr
XM_011537069.1:c.1891G>T	XP_011535371.1:p.Asp631Tyr
XM_011537070.1:c.1834G>T	XP_011535372.1:p.Asp612Tyr
XM_011537071.1:c.1801G>T	XP_011535373.1:p.Asp601Tyr
XM_011537072.1:c.1780G>T	XP_011535374.1:p.Asp594Tyr
XM_011537073.1:c.1573G>T	XP_011535375.1:p.Asp525Tyr
XM_011537074.1:c.1573G>T	XP_011535376.1:p.Asp525Tyr
XM_005267991.3:c.1987G>T	XP_005268048.2:p.Asp663Tyr
XM_005267992.3:c.1981G>T	XP_005268049.2:p.Asp661Tyr
XM_011537067.2:c.1930G>T	XP_011535369.1:p.Asp644Tyr
XM_011537069.2:c.1978G>T	XP_011535371.2:p.Asp660Tyr
XM_011537070.2:c.1834G>T	XP_011535372.1:p.Asp612Tyr
XM_011537071.2:c.1888G>T	XP_011535373.2:p.Asp630Tyr
XM_011537072.2:c.1780G>T	XP_011535374.1:p.Asp594Tyr
XM_017021582.1:c.2038G>T	XP_016877071.1:p.Asp680Tyr
XM_017021583.1:c.2029G>T	XP_016877072.1:p.Asp677Tyr
XM_017021584.1:c.1948G>T	XP_016877073.1:p.Asp650Tyr
XM_017021585.1:c.1897G>T	XP_016877074.1:p.Asp633Tyr
XM_017021586.1:c.1573G>T	XP_016877075.1:p.Asp525Tyr
XM_017021587.1:c.1573G>T	XP_016877076.1:p.Asp525Tyr
XM_017021588.1:c.1573G>T	XP_016877077.1:p.Asp525Tyr
NM_001164749.2:c.1879G>T MANE Select	NP_001158221.1:p.Asp627Tyr
NM_001165893.2:c.1789G>T	NP_001159365.1:p.Asp597Tyr
NM_022123.3:c.1783G>T	NP_071406.1:p.Asp595Tyr
NM_173159.3:c.1840G>T	NP_775182.1:p.Asp614Tyr
NM_001394988.1:c.1834G>T	NP_001381917.1:p.Asp612Tyr
NM_001394989.1:c.1780G>T	NP_001381918.1:p.Asp594Tyr