Canonical Allele Identifier: CA389413462

Gene: NPAS3

Linked Data

• gnomAD v4: 14-33800307-A-G
• MyVariant Identifiers: chr14:g.34269513A>G (hg19) ; chr14:g.33800307A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800307A>G , CM000676.2:g.33800307A>G	GRCh38
NC_000014.8:g.34269513A>G , CM000676.1:g.34269513A>G	GRCh37
NC_000014.7:g.33339264A>G	NCBI36
NG_013036.1:g.866055A>G
NG_013036.2:g.866055A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2000A>G MANE Select	ENSP00000348460.4:p.Tyr667Cys
ENST00000551634.6:c.2009A>G	ENSP00000448373.2:p.Tyr670Cys
ENST00000680362.1:c.1900A>G
ENST00000681323.1:c.793+2726A>G
ENST00000346562.6:c.1904A>G	ENSP00000319610.5:p.Tyr635Cys
ENST00000356141.8:c.2000A>G	ENSP00000348460.4:p.Tyr667Cys
ENST00000357798.9:c.1961A>G	ENSP00000350446.5:p.Tyr654Cys
ENST00000548645.5:c.1910A>G	ENSP00000448916.1:p.Tyr637Cys
ENST00000551492.5:c.2015A>G	ENSP00000450392.1:p.Tyr672Cys
ENST00000551634.5:c.1922A>G	ENSP00000448373.1:p.Tyr641Cys
NM_001164749.1:c.2000A>G	NP_001158221.1:p.Tyr667Cys
NM_001165893.1:c.1910A>G	NP_001159365.1:p.Tyr637Cys
NM_022123.2:c.1904A>G	NP_071406.1:p.Tyr635Cys
NM_173159.2:c.1961A>G	NP_775182.1:p.Tyr654Cys
XM_005267991.2:c.2021A>G	XP_005268048.1:p.Tyr674Cys
XM_005267992.2:c.2015A>G	XP_005268049.1:p.Tyr672Cys
XM_005267993.2:c.1961A>G	XP_005268050.1:p.Tyr654Cys
XM_011537067.1:c.2051A>G	XP_011535369.1:p.Tyr684Cys
XM_011537068.1:c.2042A>G	XP_011535370.1:p.Tyr681Cys
XM_011537069.1:c.2012A>G	XP_011535371.1:p.Tyr671Cys
XM_011537070.1:c.1955A>G	XP_011535372.1:p.Tyr652Cys
XM_011537071.1:c.1922A>G	XP_011535373.1:p.Tyr641Cys
XM_011537072.1:c.1901A>G	XP_011535374.1:p.Tyr634Cys
XM_011537073.1:c.1694A>G	XP_011535375.1:p.Tyr565Cys
XM_011537074.1:c.1694A>G	XP_011535376.1:p.Tyr565Cys
XM_005267991.3:c.2108A>G	XP_005268048.2:p.Tyr703Cys
XM_005267992.3:c.2102A>G	XP_005268049.2:p.Tyr701Cys
XM_011537067.2:c.2051A>G	XP_011535369.1:p.Tyr684Cys
XM_011537069.2:c.2099A>G	XP_011535371.2:p.Tyr700Cys
XM_011537070.2:c.1955A>G	XP_011535372.1:p.Tyr652Cys
XM_011537071.2:c.2009A>G	XP_011535373.2:p.Tyr670Cys
XM_011537072.2:c.1901A>G	XP_011535374.1:p.Tyr634Cys
XM_017021582.1:c.2159A>G	XP_016877071.1:p.Tyr720Cys
XM_017021583.1:c.2150A>G	XP_016877072.1:p.Tyr717Cys
XM_017021584.1:c.2069A>G	XP_016877073.1:p.Tyr690Cys
XM_017021585.1:c.2018A>G	XP_016877074.1:p.Tyr673Cys
XM_017021586.1:c.1694A>G	XP_016877075.1:p.Tyr565Cys
XM_017021587.1:c.1694A>G	XP_016877076.1:p.Tyr565Cys
XM_017021588.1:c.1694A>G	XP_016877077.1:p.Tyr565Cys
NM_001164749.2:c.2000A>G MANE Select	NP_001158221.1:p.Tyr667Cys
NM_001165893.2:c.1910A>G	NP_001159365.1:p.Tyr637Cys
NM_022123.3:c.1904A>G	NP_071406.1:p.Tyr635Cys
NM_173159.3:c.1961A>G	NP_775182.1:p.Tyr654Cys
NM_001394988.1:c.1955A>G	NP_001381917.1:p.Tyr652Cys
NM_001394989.1:c.1901A>G	NP_001381918.1:p.Tyr634Cys