Canonical Allele Identifier: CA389412684

Gene: NPAS3

Linked Data

• dbSNP Id: rs753158908
• gnomAD v3: 14-33800136-G-A
• gnomAD v4: 14-33800136-G-A
• MyVariant Identifiers: chr14:g.34269342G>A (hg19) ; chr14:g.33800136G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800136G>A , CM000676.2:g.33800136G>A	GRCh38
NC_000014.8:g.34269342G>A , CM000676.1:g.34269342G>A	GRCh37
NC_000014.7:g.33339093G>A	NCBI36
NG_013036.1:g.865884G>A
NG_013036.2:g.865884G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1829G>A MANE Select	ENSP00000348460.4:p.Gly610Asp
ENST00000551634.6:c.1838G>A	ENSP00000448373.2:p.Gly613Asp
ENST00000680362.1:c.1729G>A
ENST00000681323.1:c.793+2555G>A
ENST00000346562.6:c.1733G>A	ENSP00000319610.5:p.Gly578Asp
ENST00000356141.8:c.1829G>A	ENSP00000348460.4:p.Gly610Asp
ENST00000357798.9:c.1790G>A	ENSP00000350446.5:p.Gly597Asp
ENST00000548645.5:c.1739G>A	ENSP00000448916.1:p.Gly580Asp
ENST00000551492.5:c.1844G>A	ENSP00000450392.1:p.Gly615Asp
ENST00000551634.5:c.1751G>A	ENSP00000448373.1:p.Gly584Asp
NM_001164749.1:c.1829G>A	NP_001158221.1:p.Gly610Asp
NM_001165893.1:c.1739G>A	NP_001159365.1:p.Gly580Asp
NM_022123.2:c.1733G>A	NP_071406.1:p.Gly578Asp
NM_173159.2:c.1790G>A	NP_775182.1:p.Gly597Asp
XM_005267991.2:c.1850G>A	XP_005268048.1:p.Gly617Asp
XM_005267992.2:c.1844G>A	XP_005268049.1:p.Gly615Asp
XM_005267993.2:c.1790G>A	XP_005268050.1:p.Gly597Asp
XM_011537067.1:c.1880G>A	XP_011535369.1:p.Gly627Asp
XM_011537068.1:c.1871G>A	XP_011535370.1:p.Gly624Asp
XM_011537069.1:c.1841G>A	XP_011535371.1:p.Gly614Asp
XM_011537070.1:c.1784G>A	XP_011535372.1:p.Gly595Asp
XM_011537071.1:c.1751G>A	XP_011535373.1:p.Gly584Asp
XM_011537072.1:c.1730G>A	XP_011535374.1:p.Gly577Asp
XM_011537073.1:c.1523G>A	XP_011535375.1:p.Gly508Asp
XM_011537074.1:c.1523G>A	XP_011535376.1:p.Gly508Asp
XM_005267991.3:c.1937G>A	XP_005268048.2:p.Gly646Asp
XM_005267992.3:c.1931G>A	XP_005268049.2:p.Gly644Asp
XM_011537067.2:c.1880G>A	XP_011535369.1:p.Gly627Asp
XM_011537069.2:c.1928G>A	XP_011535371.2:p.Gly643Asp
XM_011537070.2:c.1784G>A	XP_011535372.1:p.Gly595Asp
XM_011537071.2:c.1838G>A	XP_011535373.2:p.Gly613Asp
XM_011537072.2:c.1730G>A	XP_011535374.1:p.Gly577Asp
XM_017021582.1:c.1988G>A	XP_016877071.1:p.Gly663Asp
XM_017021583.1:c.1979G>A	XP_016877072.1:p.Gly660Asp
XM_017021584.1:c.1898G>A	XP_016877073.1:p.Gly633Asp
XM_017021585.1:c.1847G>A	XP_016877074.1:p.Gly616Asp
XM_017021586.1:c.1523G>A	XP_016877075.1:p.Gly508Asp
XM_017021587.1:c.1523G>A	XP_016877076.1:p.Gly508Asp
XM_017021588.1:c.1523G>A	XP_016877077.1:p.Gly508Asp
NM_001164749.2:c.1829G>A MANE Select	NP_001158221.1:p.Gly610Asp
NM_001165893.2:c.1739G>A	NP_001159365.1:p.Gly580Asp
NM_022123.3:c.1733G>A	NP_071406.1:p.Gly578Asp
NM_173159.3:c.1790G>A	NP_775182.1:p.Gly597Asp
NM_001394988.1:c.1784G>A	NP_001381917.1:p.Gly595Asp
NM_001394989.1:c.1730G>A	NP_001381918.1:p.Gly577Asp