Canonical Allele Identifier: CA389412548

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269322G>C (hg19) ; chr14:g.33800116G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800116G>C , CM000676.2:g.33800116G>C	GRCh38
NC_000014.8:g.34269322G>C , CM000676.1:g.34269322G>C	GRCh37
NC_000014.7:g.33339073G>C	NCBI36
NG_013036.1:g.865864G>C
NG_013036.2:g.865864G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1809G>C MANE Select	ENSP00000348460.4:p.Arg603Ser
ENST00000551634.6:c.1818G>C	ENSP00000448373.2:p.Arg606Ser
ENST00000680362.1:c.1709G>C
ENST00000681323.1:c.793+2535G>C
ENST00000346562.6:c.1713G>C	ENSP00000319610.5:p.Arg571Ser
ENST00000356141.8:c.1809G>C	ENSP00000348460.4:p.Arg603Ser
ENST00000357798.9:c.1770G>C	ENSP00000350446.5:p.Arg590Ser
ENST00000548645.5:c.1719G>C	ENSP00000448916.1:p.Arg573Ser
ENST00000551492.5:c.1824G>C	ENSP00000450392.1:p.Arg608Ser
ENST00000551634.5:c.1731G>C	ENSP00000448373.1:p.Arg577Ser
NM_001164749.1:c.1809G>C	NP_001158221.1:p.Arg603Ser
NM_001165893.1:c.1719G>C	NP_001159365.1:p.Arg573Ser
NM_022123.2:c.1713G>C	NP_071406.1:p.Arg571Ser
NM_173159.2:c.1770G>C	NP_775182.1:p.Arg590Ser
XM_005267991.2:c.1830G>C	XP_005268048.1:p.Arg610Ser
XM_005267992.2:c.1824G>C	XP_005268049.1:p.Arg608Ser
XM_005267993.2:c.1770G>C	XP_005268050.1:p.Arg590Ser
XM_011537067.1:c.1860G>C	XP_011535369.1:p.Arg620Ser
XM_011537068.1:c.1851G>C	XP_011535370.1:p.Arg617Ser
XM_011537069.1:c.1821G>C	XP_011535371.1:p.Arg607Ser
XM_011537070.1:c.1764G>C	XP_011535372.1:p.Arg588Ser
XM_011537071.1:c.1731G>C	XP_011535373.1:p.Arg577Ser
XM_011537072.1:c.1710G>C	XP_011535374.1:p.Arg570Ser
XM_011537073.1:c.1503G>C	XP_011535375.1:p.Arg501Ser
XM_011537074.1:c.1503G>C	XP_011535376.1:p.Arg501Ser
XM_005267991.3:c.1917G>C	XP_005268048.2:p.Arg639Ser
XM_005267992.3:c.1911G>C	XP_005268049.2:p.Arg637Ser
XM_011537067.2:c.1860G>C	XP_011535369.1:p.Arg620Ser
XM_011537069.2:c.1908G>C	XP_011535371.2:p.Arg636Ser
XM_011537070.2:c.1764G>C	XP_011535372.1:p.Arg588Ser
XM_011537071.2:c.1818G>C	XP_011535373.2:p.Arg606Ser
XM_011537072.2:c.1710G>C	XP_011535374.1:p.Arg570Ser
XM_017021582.1:c.1968G>C	XP_016877071.1:p.Arg656Ser
XM_017021583.1:c.1959G>C	XP_016877072.1:p.Arg653Ser
XM_017021584.1:c.1878G>C	XP_016877073.1:p.Arg626Ser
XM_017021585.1:c.1827G>C	XP_016877074.1:p.Arg609Ser
XM_017021586.1:c.1503G>C	XP_016877075.1:p.Arg501Ser
XM_017021587.1:c.1503G>C	XP_016877076.1:p.Arg501Ser
XM_017021588.1:c.1503G>C	XP_016877077.1:p.Arg501Ser
NM_001164749.2:c.1809G>C MANE Select	NP_001158221.1:p.Arg603Ser
NM_001165893.2:c.1719G>C	NP_001159365.1:p.Arg573Ser
NM_022123.3:c.1713G>C	NP_071406.1:p.Arg571Ser
NM_173159.3:c.1770G>C	NP_775182.1:p.Arg590Ser
NM_001394988.1:c.1764G>C	NP_001381917.1:p.Arg588Ser
NM_001394989.1:c.1710G>C	NP_001381918.1:p.Arg570Ser