Canonical Allele Identifier: CA389412539

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269320A>T (hg19) ; chr14:g.33800114A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800114A>T , CM000676.2:g.33800114A>T	GRCh38
NC_000014.8:g.34269320A>T , CM000676.1:g.34269320A>T	GRCh37
NC_000014.7:g.33339071A>T	NCBI36
NG_013036.1:g.865862A>T
NG_013036.2:g.865862A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1807A>T MANE Select	ENSP00000348460.4:p.Arg603Trp
ENST00000551634.6:c.1816A>T	ENSP00000448373.2:p.Arg606Trp
ENST00000680362.1:c.1707A>T
ENST00000681323.1:c.793+2533A>T
ENST00000346562.6:c.1711A>T	ENSP00000319610.5:p.Arg571Trp
ENST00000356141.8:c.1807A>T	ENSP00000348460.4:p.Arg603Trp
ENST00000357798.9:c.1768A>T	ENSP00000350446.5:p.Arg590Trp
ENST00000548645.5:c.1717A>T	ENSP00000448916.1:p.Arg573Trp
ENST00000551492.5:c.1822A>T	ENSP00000450392.1:p.Arg608Trp
ENST00000551634.5:c.1729A>T	ENSP00000448373.1:p.Arg577Trp
NM_001164749.1:c.1807A>T	NP_001158221.1:p.Arg603Trp
NM_001165893.1:c.1717A>T	NP_001159365.1:p.Arg573Trp
NM_022123.2:c.1711A>T	NP_071406.1:p.Arg571Trp
NM_173159.2:c.1768A>T	NP_775182.1:p.Arg590Trp
XM_005267991.2:c.1828A>T	XP_005268048.1:p.Arg610Trp
XM_005267992.2:c.1822A>T	XP_005268049.1:p.Arg608Trp
XM_005267993.2:c.1768A>T	XP_005268050.1:p.Arg590Trp
XM_011537067.1:c.1858A>T	XP_011535369.1:p.Arg620Trp
XM_011537068.1:c.1849A>T	XP_011535370.1:p.Arg617Trp
XM_011537069.1:c.1819A>T	XP_011535371.1:p.Arg607Trp
XM_011537070.1:c.1762A>T	XP_011535372.1:p.Arg588Trp
XM_011537071.1:c.1729A>T	XP_011535373.1:p.Arg577Trp
XM_011537072.1:c.1708A>T	XP_011535374.1:p.Arg570Trp
XM_011537073.1:c.1501A>T	XP_011535375.1:p.Arg501Trp
XM_011537074.1:c.1501A>T	XP_011535376.1:p.Arg501Trp
XM_005267991.3:c.1915A>T	XP_005268048.2:p.Arg639Trp
XM_005267992.3:c.1909A>T	XP_005268049.2:p.Arg637Trp
XM_011537067.2:c.1858A>T	XP_011535369.1:p.Arg620Trp
XM_011537069.2:c.1906A>T	XP_011535371.2:p.Arg636Trp
XM_011537070.2:c.1762A>T	XP_011535372.1:p.Arg588Trp
XM_011537071.2:c.1816A>T	XP_011535373.2:p.Arg606Trp
XM_011537072.2:c.1708A>T	XP_011535374.1:p.Arg570Trp
XM_017021582.1:c.1966A>T	XP_016877071.1:p.Arg656Trp
XM_017021583.1:c.1957A>T	XP_016877072.1:p.Arg653Trp
XM_017021584.1:c.1876A>T	XP_016877073.1:p.Arg626Trp
XM_017021585.1:c.1825A>T	XP_016877074.1:p.Arg609Trp
XM_017021586.1:c.1501A>T	XP_016877075.1:p.Arg501Trp
XM_017021587.1:c.1501A>T	XP_016877076.1:p.Arg501Trp
XM_017021588.1:c.1501A>T	XP_016877077.1:p.Arg501Trp
NM_001164749.2:c.1807A>T MANE Select	NP_001158221.1:p.Arg603Trp
NM_001165893.2:c.1717A>T	NP_001159365.1:p.Arg573Trp
NM_022123.3:c.1711A>T	NP_071406.1:p.Arg571Trp
NM_173159.3:c.1768A>T	NP_775182.1:p.Arg590Trp
NM_001394988.1:c.1762A>T	NP_001381917.1:p.Arg588Trp
NM_001394989.1:c.1708A>T	NP_001381918.1:p.Arg570Trp