Canonical Allele Identifier: CA389412798

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269360G>C (hg19) ; chr14:g.33800154G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800154G>C , CM000676.2:g.33800154G>C	GRCh38
NC_000014.8:g.34269360G>C , CM000676.1:g.34269360G>C	GRCh37
NC_000014.7:g.33339111G>C	NCBI36
NG_013036.1:g.865902G>C
NG_013036.2:g.865902G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1847G>C MANE Select	ENSP00000348460.4:p.Arg616Pro
ENST00000551634.6:c.1856G>C	ENSP00000448373.2:p.Arg619Pro
ENST00000680362.1:c.1747G>C
ENST00000681323.1:c.793+2573G>C
ENST00000346562.6:c.1751G>C	ENSP00000319610.5:p.Arg584Pro
ENST00000356141.8:c.1847G>C	ENSP00000348460.4:p.Arg616Pro
ENST00000357798.9:c.1808G>C	ENSP00000350446.5:p.Arg603Pro
ENST00000548645.5:c.1757G>C	ENSP00000448916.1:p.Arg586Pro
ENST00000551492.5:c.1862G>C	ENSP00000450392.1:p.Arg621Pro
ENST00000551634.5:c.1769G>C	ENSP00000448373.1:p.Arg590Pro
NM_001164749.1:c.1847G>C	NP_001158221.1:p.Arg616Pro
NM_001165893.1:c.1757G>C	NP_001159365.1:p.Arg586Pro
NM_022123.2:c.1751G>C	NP_071406.1:p.Arg584Pro
NM_173159.2:c.1808G>C	NP_775182.1:p.Arg603Pro
XM_005267991.2:c.1868G>C	XP_005268048.1:p.Arg623Pro
XM_005267992.2:c.1862G>C	XP_005268049.1:p.Arg621Pro
XM_005267993.2:c.1808G>C	XP_005268050.1:p.Arg603Pro
XM_011537067.1:c.1898G>C	XP_011535369.1:p.Arg633Pro
XM_011537068.1:c.1889G>C	XP_011535370.1:p.Arg630Pro
XM_011537069.1:c.1859G>C	XP_011535371.1:p.Arg620Pro
XM_011537070.1:c.1802G>C	XP_011535372.1:p.Arg601Pro
XM_011537071.1:c.1769G>C	XP_011535373.1:p.Arg590Pro
XM_011537072.1:c.1748G>C	XP_011535374.1:p.Arg583Pro
XM_011537073.1:c.1541G>C	XP_011535375.1:p.Arg514Pro
XM_011537074.1:c.1541G>C	XP_011535376.1:p.Arg514Pro
XM_005267991.3:c.1955G>C	XP_005268048.2:p.Arg652Pro
XM_005267992.3:c.1949G>C	XP_005268049.2:p.Arg650Pro
XM_011537067.2:c.1898G>C	XP_011535369.1:p.Arg633Pro
XM_011537069.2:c.1946G>C	XP_011535371.2:p.Arg649Pro
XM_011537070.2:c.1802G>C	XP_011535372.1:p.Arg601Pro
XM_011537071.2:c.1856G>C	XP_011535373.2:p.Arg619Pro
XM_011537072.2:c.1748G>C	XP_011535374.1:p.Arg583Pro
XM_017021582.1:c.2006G>C	XP_016877071.1:p.Arg669Pro
XM_017021583.1:c.1997G>C	XP_016877072.1:p.Arg666Pro
XM_017021584.1:c.1916G>C	XP_016877073.1:p.Arg639Pro
XM_017021585.1:c.1865G>C	XP_016877074.1:p.Arg622Pro
XM_017021586.1:c.1541G>C	XP_016877075.1:p.Arg514Pro
XM_017021587.1:c.1541G>C	XP_016877076.1:p.Arg514Pro
XM_017021588.1:c.1541G>C	XP_016877077.1:p.Arg514Pro
NM_001164749.2:c.1847G>C MANE Select	NP_001158221.1:p.Arg616Pro
NM_001165893.2:c.1757G>C	NP_001159365.1:p.Arg586Pro
NM_022123.3:c.1751G>C	NP_071406.1:p.Arg584Pro
NM_173159.3:c.1808G>C	NP_775182.1:p.Arg603Pro
NM_001394988.1:c.1802G>C	NP_001381917.1:p.Arg601Pro
NM_001394989.1:c.1748G>C	NP_001381918.1:p.Arg583Pro