Canonical Allele Identifier: CA2128327149

Gene: NPAS3

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800243C= , CM000676.2:g.33800243C=	GRCh38
NC_000014.8:g.34269449C= , CM000676.1:g.34269449C=	GRCh37
NC_000014.7:g.33339200C=	NCBI36
NG_013036.1:g.865991C=
NG_013036.2:g.865991C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1936C= MANE Select	ENSP00000348460.4:p.Leu646=
ENST00000551634.6:c.1945C=	ENSP00000448373.2:p.Leu649=
ENST00000680362.1:c.1836C=
ENST00000681323.1:c.793+2662C=
ENST00000346562.6:c.1840C=	ENSP00000319610.5:p.Leu614=
ENST00000356141.8:c.1936C=	ENSP00000348460.4:p.Leu646=
ENST00000357798.9:c.1897C=	ENSP00000350446.5:p.Leu633=
ENST00000548645.5:c.1846C=	ENSP00000448916.1:p.Leu616=
ENST00000551492.5:c.1951C=	ENSP00000450392.1:p.Leu651=
ENST00000551634.5:c.1858C=	ENSP00000448373.1:p.Leu620=
NM_001164749.1:c.1936C=	NP_001158221.1:p.Leu646=
NM_001165893.1:c.1846C=	NP_001159365.1:p.Leu616=
NM_022123.2:c.1840C=	NP_071406.1:p.Leu614=
NM_173159.2:c.1897C=	NP_775182.1:p.Leu633=
XM_005267991.2:c.1957C=	XP_005268048.1:p.Leu653=
XM_005267992.2:c.1951C=	XP_005268049.1:p.Leu651=
XM_005267993.2:c.1897C=	XP_005268050.1:p.Leu633=
XM_011537067.1:c.1987C=	XP_011535369.1:p.Leu663=
XM_011537068.1:c.1978C=	XP_011535370.1:p.Leu660=
XM_011537069.1:c.1948C=	XP_011535371.1:p.Leu650=
XM_011537070.1:c.1891C=	XP_011535372.1:p.Leu631=
XM_011537071.1:c.1858C=	XP_011535373.1:p.Leu620=
XM_011537072.1:c.1837C=	XP_011535374.1:p.Leu613=
XM_011537073.1:c.1630C=	XP_011535375.1:p.Leu544=
XM_011537074.1:c.1630C=	XP_011535376.1:p.Leu544=
XM_005267991.3:c.2044C=	XP_005268048.2:p.Leu682=
XM_005267992.3:c.2038C=	XP_005268049.2:p.Leu680=
XM_011537067.2:c.1987C=	XP_011535369.1:p.Leu663=
XM_011537069.2:c.2035C=	XP_011535371.2:p.Leu679=
XM_011537070.2:c.1891C=	XP_011535372.1:p.Leu631=
XM_011537071.2:c.1945C=	XP_011535373.2:p.Leu649=
XM_011537072.2:c.1837C=	XP_011535374.1:p.Leu613=
XM_017021582.1:c.2095C=	XP_016877071.1:p.Leu699=
XM_017021583.1:c.2086C=	XP_016877072.1:p.Leu696=
XM_017021584.1:c.2005C=	XP_016877073.1:p.Leu669=
XM_017021585.1:c.1954C=	XP_016877074.1:p.Leu652=
XM_017021586.1:c.1630C=	XP_016877075.1:p.Leu544=
XM_017021587.1:c.1630C=	XP_016877076.1:p.Leu544=
XM_017021588.1:c.1630C=	XP_016877077.1:p.Leu544=
NM_001164749.2:c.1936C= MANE Select	NP_001158221.1:p.Leu646=
NM_001165893.2:c.1846C=	NP_001159365.1:p.Leu616=
NM_022123.3:c.1840C=	NP_071406.1:p.Leu614=
NM_173159.3:c.1897C=	NP_775182.1:p.Leu633=
NM_001394988.1:c.1891C=	NP_001381917.1:p.Leu631=
NM_001394989.1:c.1837C=	NP_001381918.1:p.Leu613=