Canonical Allele Identifier: CA389413518

Gene: NPAS3

Linked Data

• gnomAD v4: 14-33800321-G-T
• MyVariant Identifiers: chr14:g.34269527G>T (hg19) ; chr14:g.33800321G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800321G>T , CM000676.2:g.33800321G>T	GRCh38
NC_000014.8:g.34269527G>T , CM000676.1:g.34269527G>T	GRCh37
NC_000014.7:g.33339278G>T	NCBI36
NG_013036.1:g.866069G>T
NG_013036.2:g.866069G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2014G>T MANE Select	ENSP00000348460.4:p.Glu672Ter
ENST00000551634.6:c.2023G>T	ENSP00000448373.2:p.Glu675Ter
ENST00000680362.1:c.1914G>T
ENST00000681323.1:c.793+2740G>T
ENST00000346562.6:c.1918G>T	ENSP00000319610.5:p.Glu640Ter
ENST00000356141.8:c.2014G>T	ENSP00000348460.4:p.Glu672Ter
ENST00000357798.9:c.1975G>T	ENSP00000350446.5:p.Glu659Ter
ENST00000548645.5:c.1924G>T	ENSP00000448916.1:p.Glu642Ter
ENST00000551492.5:c.2029G>T	ENSP00000450392.1:p.Glu677Ter
ENST00000551634.5:c.1936G>T	ENSP00000448373.1:p.Glu646Ter
NM_001164749.1:c.2014G>T	NP_001158221.1:p.Glu672Ter
NM_001165893.1:c.1924G>T	NP_001159365.1:p.Glu642Ter
NM_022123.2:c.1918G>T	NP_071406.1:p.Glu640Ter
NM_173159.2:c.1975G>T	NP_775182.1:p.Glu659Ter
XM_005267991.2:c.2035G>T	XP_005268048.1:p.Glu679Ter
XM_005267992.2:c.2029G>T	XP_005268049.1:p.Glu677Ter
XM_005267993.2:c.1975G>T	XP_005268050.1:p.Glu659Ter
XM_011537067.1:c.2065G>T	XP_011535369.1:p.Glu689Ter
XM_011537068.1:c.2056G>T	XP_011535370.1:p.Glu686Ter
XM_011537069.1:c.2026G>T	XP_011535371.1:p.Glu676Ter
XM_011537070.1:c.1969G>T	XP_011535372.1:p.Glu657Ter
XM_011537071.1:c.1936G>T	XP_011535373.1:p.Glu646Ter
XM_011537072.1:c.1915G>T	XP_011535374.1:p.Glu639Ter
XM_011537073.1:c.1708G>T	XP_011535375.1:p.Glu570Ter
XM_011537074.1:c.1708G>T	XP_011535376.1:p.Glu570Ter
XM_005267991.3:c.2122G>T	XP_005268048.2:p.Glu708Ter
XM_005267992.3:c.2116G>T	XP_005268049.2:p.Glu706Ter
XM_011537067.2:c.2065G>T	XP_011535369.1:p.Glu689Ter
XM_011537069.2:c.2113G>T	XP_011535371.2:p.Glu705Ter
XM_011537070.2:c.1969G>T	XP_011535372.1:p.Glu657Ter
XM_011537071.2:c.2023G>T	XP_011535373.2:p.Glu675Ter
XM_011537072.2:c.1915G>T	XP_011535374.1:p.Glu639Ter
XM_017021582.1:c.2173G>T	XP_016877071.1:p.Glu725Ter
XM_017021583.1:c.2164G>T	XP_016877072.1:p.Glu722Ter
XM_017021584.1:c.2083G>T	XP_016877073.1:p.Glu695Ter
XM_017021585.1:c.2032G>T	XP_016877074.1:p.Glu678Ter
XM_017021586.1:c.1708G>T	XP_016877075.1:p.Glu570Ter
XM_017021587.1:c.1708G>T	XP_016877076.1:p.Glu570Ter
XM_017021588.1:c.1708G>T	XP_016877077.1:p.Glu570Ter
NM_001164749.2:c.2014G>T MANE Select	NP_001158221.1:p.Glu672Ter
NM_001165893.2:c.1924G>T	NP_001159365.1:p.Glu642Ter
NM_022123.3:c.1918G>T	NP_071406.1:p.Glu640Ter
NM_173159.3:c.1975G>T	NP_775182.1:p.Glu659Ter
NM_001394988.1:c.1969G>T	NP_001381917.1:p.Glu657Ter
NM_001394989.1:c.1915G>T	NP_001381918.1:p.Glu639Ter