Canonical Allele Identifier: CA389412536

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269319A>C (hg19) ; chr14:g.33800113A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800113A>C , CM000676.2:g.33800113A>C	GRCh38
NC_000014.8:g.34269319A>C , CM000676.1:g.34269319A>C	GRCh37
NC_000014.7:g.33339070A>C	NCBI36
NG_013036.1:g.865861A>C
NG_013036.2:g.865861A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1806A>C MANE Select	ENSP00000348460.4:p.Lys602Asn
ENST00000551634.6:c.1815A>C	ENSP00000448373.2:p.Lys605Asn
ENST00000680362.1:c.1706A>C
ENST00000681323.1:c.793+2532A>C
ENST00000346562.6:c.1710A>C	ENSP00000319610.5:p.Lys570Asn
ENST00000356141.8:c.1806A>C	ENSP00000348460.4:p.Lys602Asn
ENST00000357798.9:c.1767A>C	ENSP00000350446.5:p.Lys589Asn
ENST00000548645.5:c.1716A>C	ENSP00000448916.1:p.Lys572Asn
ENST00000551492.5:c.1821A>C	ENSP00000450392.1:p.Lys607Asn
ENST00000551634.5:c.1728A>C	ENSP00000448373.1:p.Lys576Asn
NM_001164749.1:c.1806A>C	NP_001158221.1:p.Lys602Asn
NM_001165893.1:c.1716A>C	NP_001159365.1:p.Lys572Asn
NM_022123.2:c.1710A>C	NP_071406.1:p.Lys570Asn
NM_173159.2:c.1767A>C	NP_775182.1:p.Lys589Asn
XM_005267991.2:c.1827A>C	XP_005268048.1:p.Lys609Asn
XM_005267992.2:c.1821A>C	XP_005268049.1:p.Lys607Asn
XM_005267993.2:c.1767A>C	XP_005268050.1:p.Lys589Asn
XM_011537067.1:c.1857A>C	XP_011535369.1:p.Lys619Asn
XM_011537068.1:c.1848A>C	XP_011535370.1:p.Lys616Asn
XM_011537069.1:c.1818A>C	XP_011535371.1:p.Lys606Asn
XM_011537070.1:c.1761A>C	XP_011535372.1:p.Lys587Asn
XM_011537071.1:c.1728A>C	XP_011535373.1:p.Lys576Asn
XM_011537072.1:c.1707A>C	XP_011535374.1:p.Lys569Asn
XM_011537073.1:c.1500A>C	XP_011535375.1:p.Lys500Asn
XM_011537074.1:c.1500A>C	XP_011535376.1:p.Lys500Asn
XM_005267991.3:c.1914A>C	XP_005268048.2:p.Lys638Asn
XM_005267992.3:c.1908A>C	XP_005268049.2:p.Lys636Asn
XM_011537067.2:c.1857A>C	XP_011535369.1:p.Lys619Asn
XM_011537069.2:c.1905A>C	XP_011535371.2:p.Lys635Asn
XM_011537070.2:c.1761A>C	XP_011535372.1:p.Lys587Asn
XM_011537071.2:c.1815A>C	XP_011535373.2:p.Lys605Asn
XM_011537072.2:c.1707A>C	XP_011535374.1:p.Lys569Asn
XM_017021582.1:c.1965A>C	XP_016877071.1:p.Lys655Asn
XM_017021583.1:c.1956A>C	XP_016877072.1:p.Lys652Asn
XM_017021584.1:c.1875A>C	XP_016877073.1:p.Lys625Asn
XM_017021585.1:c.1824A>C	XP_016877074.1:p.Lys608Asn
XM_017021586.1:c.1500A>C	XP_016877075.1:p.Lys500Asn
XM_017021587.1:c.1500A>C	XP_016877076.1:p.Lys500Asn
XM_017021588.1:c.1500A>C	XP_016877077.1:p.Lys500Asn
NM_001164749.2:c.1806A>C MANE Select	NP_001158221.1:p.Lys602Asn
NM_001165893.2:c.1716A>C	NP_001159365.1:p.Lys572Asn
NM_022123.3:c.1710A>C	NP_071406.1:p.Lys570Asn
NM_173159.3:c.1767A>C	NP_775182.1:p.Lys589Asn
NM_001394988.1:c.1761A>C	NP_001381917.1:p.Lys587Asn
NM_001394989.1:c.1707A>C	NP_001381918.1:p.Lys569Asn