Canonical Allele Identifier: CA389412545

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269321G>C (hg19) ; chr14:g.33800115G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800115G>C , CM000676.2:g.33800115G>C	GRCh38
NC_000014.8:g.34269321G>C , CM000676.1:g.34269321G>C	GRCh37
NC_000014.7:g.33339072G>C	NCBI36
NG_013036.1:g.865863G>C
NG_013036.2:g.865863G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1808G>C MANE Select	ENSP00000348460.4:p.Arg603Thr
ENST00000551634.6:c.1817G>C	ENSP00000448373.2:p.Arg606Thr
ENST00000680362.1:c.1708G>C
ENST00000681323.1:c.793+2534G>C
ENST00000346562.6:c.1712G>C	ENSP00000319610.5:p.Arg571Thr
ENST00000356141.8:c.1808G>C	ENSP00000348460.4:p.Arg603Thr
ENST00000357798.9:c.1769G>C	ENSP00000350446.5:p.Arg590Thr
ENST00000548645.5:c.1718G>C	ENSP00000448916.1:p.Arg573Thr
ENST00000551492.5:c.1823G>C	ENSP00000450392.1:p.Arg608Thr
ENST00000551634.5:c.1730G>C	ENSP00000448373.1:p.Arg577Thr
NM_001164749.1:c.1808G>C	NP_001158221.1:p.Arg603Thr
NM_001165893.1:c.1718G>C	NP_001159365.1:p.Arg573Thr
NM_022123.2:c.1712G>C	NP_071406.1:p.Arg571Thr
NM_173159.2:c.1769G>C	NP_775182.1:p.Arg590Thr
XM_005267991.2:c.1829G>C	XP_005268048.1:p.Arg610Thr
XM_005267992.2:c.1823G>C	XP_005268049.1:p.Arg608Thr
XM_005267993.2:c.1769G>C	XP_005268050.1:p.Arg590Thr
XM_011537067.1:c.1859G>C	XP_011535369.1:p.Arg620Thr
XM_011537068.1:c.1850G>C	XP_011535370.1:p.Arg617Thr
XM_011537069.1:c.1820G>C	XP_011535371.1:p.Arg607Thr
XM_011537070.1:c.1763G>C	XP_011535372.1:p.Arg588Thr
XM_011537071.1:c.1730G>C	XP_011535373.1:p.Arg577Thr
XM_011537072.1:c.1709G>C	XP_011535374.1:p.Arg570Thr
XM_011537073.1:c.1502G>C	XP_011535375.1:p.Arg501Thr
XM_011537074.1:c.1502G>C	XP_011535376.1:p.Arg501Thr
XM_005267991.3:c.1916G>C	XP_005268048.2:p.Arg639Thr
XM_005267992.3:c.1910G>C	XP_005268049.2:p.Arg637Thr
XM_011537067.2:c.1859G>C	XP_011535369.1:p.Arg620Thr
XM_011537069.2:c.1907G>C	XP_011535371.2:p.Arg636Thr
XM_011537070.2:c.1763G>C	XP_011535372.1:p.Arg588Thr
XM_011537071.2:c.1817G>C	XP_011535373.2:p.Arg606Thr
XM_011537072.2:c.1709G>C	XP_011535374.1:p.Arg570Thr
XM_017021582.1:c.1967G>C	XP_016877071.1:p.Arg656Thr
XM_017021583.1:c.1958G>C	XP_016877072.1:p.Arg653Thr
XM_017021584.1:c.1877G>C	XP_016877073.1:p.Arg626Thr
XM_017021585.1:c.1826G>C	XP_016877074.1:p.Arg609Thr
XM_017021586.1:c.1502G>C	XP_016877075.1:p.Arg501Thr
XM_017021587.1:c.1502G>C	XP_016877076.1:p.Arg501Thr
XM_017021588.1:c.1502G>C	XP_016877077.1:p.Arg501Thr
NM_001164749.2:c.1808G>C MANE Select	NP_001158221.1:p.Arg603Thr
NM_001165893.2:c.1718G>C	NP_001159365.1:p.Arg573Thr
NM_022123.3:c.1712G>C	NP_071406.1:p.Arg571Thr
NM_173159.3:c.1769G>C	NP_775182.1:p.Arg590Thr
NM_001394988.1:c.1763G>C	NP_001381917.1:p.Arg588Thr
NM_001394989.1:c.1709G>C	NP_001381918.1:p.Arg570Thr