Canonical Allele Identifier: CA389413734

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269573G>A (hg19) ; chr14:g.33800367G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800367G>A , CM000676.2:g.33800367G>A	GRCh38
NC_000014.8:g.34269573G>A , CM000676.1:g.34269573G>A	GRCh37
NC_000014.7:g.33339324G>A	NCBI36
NG_013036.1:g.866115G>A
NG_013036.2:g.866115G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2060G>A MANE Select	ENSP00000348460.4:p.Ser687Asn
ENST00000551634.6:c.2069G>A	ENSP00000448373.2:p.Ser690Asn
ENST00000680362.1:c.1960G>A
ENST00000681323.1:c.793+2786G>A
ENST00000346562.6:c.1964G>A	ENSP00000319610.5:p.Ser655Asn
ENST00000356141.8:c.2060G>A	ENSP00000348460.4:p.Ser687Asn
ENST00000357798.9:c.2021G>A	ENSP00000350446.5:p.Ser674Asn
ENST00000548645.5:c.1970G>A	ENSP00000448916.1:p.Ser657Asn
ENST00000551492.5:c.2075G>A	ENSP00000450392.1:p.Ser692Asn
ENST00000551634.5:c.1982G>A	ENSP00000448373.1:p.Ser661Asn
NM_001164749.1:c.2060G>A	NP_001158221.1:p.Ser687Asn
NM_001165893.1:c.1970G>A	NP_001159365.1:p.Ser657Asn
NM_022123.2:c.1964G>A	NP_071406.1:p.Ser655Asn
NM_173159.2:c.2021G>A	NP_775182.1:p.Ser674Asn
XM_005267991.2:c.2081G>A	XP_005268048.1:p.Ser694Asn
XM_005267992.2:c.2075G>A	XP_005268049.1:p.Ser692Asn
XM_005267993.2:c.2021G>A	XP_005268050.1:p.Ser674Asn
XM_011537067.1:c.2111G>A	XP_011535369.1:p.Ser704Asn
XM_011537068.1:c.2102G>A	XP_011535370.1:p.Ser701Asn
XM_011537069.1:c.2072G>A	XP_011535371.1:p.Ser691Asn
XM_011537070.1:c.2015G>A	XP_011535372.1:p.Ser672Asn
XM_011537071.1:c.1982G>A	XP_011535373.1:p.Ser661Asn
XM_011537072.1:c.1961G>A	XP_011535374.1:p.Ser654Asn
XM_011537073.1:c.1754G>A	XP_011535375.1:p.Ser585Asn
XM_011537074.1:c.1754G>A	XP_011535376.1:p.Ser585Asn
XM_005267991.3:c.2168G>A	XP_005268048.2:p.Ser723Asn
XM_005267992.3:c.2162G>A	XP_005268049.2:p.Ser721Asn
XM_011537067.2:c.2111G>A	XP_011535369.1:p.Ser704Asn
XM_011537069.2:c.2159G>A	XP_011535371.2:p.Ser720Asn
XM_011537070.2:c.2015G>A	XP_011535372.1:p.Ser672Asn
XM_011537071.2:c.2069G>A	XP_011535373.2:p.Ser690Asn
XM_011537072.2:c.1961G>A	XP_011535374.1:p.Ser654Asn
XM_017021582.1:c.2219G>A	XP_016877071.1:p.Ser740Asn
XM_017021583.1:c.2210G>A	XP_016877072.1:p.Ser737Asn
XM_017021584.1:c.2129G>A	XP_016877073.1:p.Ser710Asn
XM_017021585.1:c.2078G>A	XP_016877074.1:p.Ser693Asn
XM_017021586.1:c.1754G>A	XP_016877075.1:p.Ser585Asn
XM_017021587.1:c.1754G>A	XP_016877076.1:p.Ser585Asn
XM_017021588.1:c.1754G>A	XP_016877077.1:p.Ser585Asn
NM_001164749.2:c.2060G>A MANE Select	NP_001158221.1:p.Ser687Asn
NM_001165893.2:c.1970G>A	NP_001159365.1:p.Ser657Asn
NM_022123.3:c.1964G>A	NP_071406.1:p.Ser655Asn
NM_173159.3:c.2021G>A	NP_775182.1:p.Ser674Asn
NM_001394988.1:c.2015G>A	NP_001381917.1:p.Ser672Asn
NM_001394989.1:c.1961G>A	NP_001381918.1:p.Ser654Asn