Canonical Allele Identifier: CA389412873

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269375C>G (hg19) ; chr14:g.33800169C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800169C>G , CM000676.2:g.33800169C>G	GRCh38
NC_000014.8:g.34269375C>G , CM000676.1:g.34269375C>G	GRCh37
NC_000014.7:g.33339126C>G	NCBI36
NG_013036.1:g.865917C>G
NG_013036.2:g.865917C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1862C>G MANE Select	ENSP00000348460.4:p.Ser621Trp
ENST00000551634.6:c.1871C>G	ENSP00000448373.2:p.Ser624Trp
ENST00000680362.1:c.1762C>G
ENST00000681323.1:c.793+2588C>G
ENST00000346562.6:c.1766C>G	ENSP00000319610.5:p.Ser589Trp
ENST00000356141.8:c.1862C>G	ENSP00000348460.4:p.Ser621Trp
ENST00000357798.9:c.1823C>G	ENSP00000350446.5:p.Ser608Trp
ENST00000548645.5:c.1772C>G	ENSP00000448916.1:p.Ser591Trp
ENST00000551492.5:c.1877C>G	ENSP00000450392.1:p.Ser626Trp
ENST00000551634.5:c.1784C>G	ENSP00000448373.1:p.Ser595Trp
NM_001164749.1:c.1862C>G	NP_001158221.1:p.Ser621Trp
NM_001165893.1:c.1772C>G	NP_001159365.1:p.Ser591Trp
NM_022123.2:c.1766C>G	NP_071406.1:p.Ser589Trp
NM_173159.2:c.1823C>G	NP_775182.1:p.Ser608Trp
XM_005267991.2:c.1883C>G	XP_005268048.1:p.Ser628Trp
XM_005267992.2:c.1877C>G	XP_005268049.1:p.Ser626Trp
XM_005267993.2:c.1823C>G	XP_005268050.1:p.Ser608Trp
XM_011537067.1:c.1913C>G	XP_011535369.1:p.Ser638Trp
XM_011537068.1:c.1904C>G	XP_011535370.1:p.Ser635Trp
XM_011537069.1:c.1874C>G	XP_011535371.1:p.Ser625Trp
XM_011537070.1:c.1817C>G	XP_011535372.1:p.Ser606Trp
XM_011537071.1:c.1784C>G	XP_011535373.1:p.Ser595Trp
XM_011537072.1:c.1763C>G	XP_011535374.1:p.Ser588Trp
XM_011537073.1:c.1556C>G	XP_011535375.1:p.Ser519Trp
XM_011537074.1:c.1556C>G	XP_011535376.1:p.Ser519Trp
XM_005267991.3:c.1970C>G	XP_005268048.2:p.Ser657Trp
XM_005267992.3:c.1964C>G	XP_005268049.2:p.Ser655Trp
XM_011537067.2:c.1913C>G	XP_011535369.1:p.Ser638Trp
XM_011537069.2:c.1961C>G	XP_011535371.2:p.Ser654Trp
XM_011537070.2:c.1817C>G	XP_011535372.1:p.Ser606Trp
XM_011537071.2:c.1871C>G	XP_011535373.2:p.Ser624Trp
XM_011537072.2:c.1763C>G	XP_011535374.1:p.Ser588Trp
XM_017021582.1:c.2021C>G	XP_016877071.1:p.Ser674Trp
XM_017021583.1:c.2012C>G	XP_016877072.1:p.Ser671Trp
XM_017021584.1:c.1931C>G	XP_016877073.1:p.Ser644Trp
XM_017021585.1:c.1880C>G	XP_016877074.1:p.Ser627Trp
XM_017021586.1:c.1556C>G	XP_016877075.1:p.Ser519Trp
XM_017021587.1:c.1556C>G	XP_016877076.1:p.Ser519Trp
XM_017021588.1:c.1556C>G	XP_016877077.1:p.Ser519Trp
NM_001164749.2:c.1862C>G MANE Select	NP_001158221.1:p.Ser621Trp
NM_001165893.2:c.1772C>G	NP_001159365.1:p.Ser591Trp
NM_022123.3:c.1766C>G	NP_071406.1:p.Ser589Trp
NM_173159.3:c.1823C>G	NP_775182.1:p.Ser608Trp
NM_001394988.1:c.1817C>G	NP_001381917.1:p.Ser606Trp
NM_001394989.1:c.1763C>G	NP_001381918.1:p.Ser588Trp