Canonical Allele Identifier: CA389413630

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269551T>G (hg19) ; chr14:g.33800345T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800345T>G , CM000676.2:g.33800345T>G	GRCh38
NC_000014.8:g.34269551T>G , CM000676.1:g.34269551T>G	GRCh37
NC_000014.7:g.33339302T>G	NCBI36
NG_013036.1:g.866093T>G
NG_013036.2:g.866093T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2038T>G MANE Select	ENSP00000348460.4:p.Tyr680Asp
ENST00000551634.6:c.2047T>G	ENSP00000448373.2:p.Tyr683Asp
ENST00000680362.1:c.1938T>G
ENST00000681323.1:c.793+2764T>G
ENST00000346562.6:c.1942T>G	ENSP00000319610.5:p.Tyr648Asp
ENST00000356141.8:c.2038T>G	ENSP00000348460.4:p.Tyr680Asp
ENST00000357798.9:c.1999T>G	ENSP00000350446.5:p.Tyr667Asp
ENST00000548645.5:c.1948T>G	ENSP00000448916.1:p.Tyr650Asp
ENST00000551492.5:c.2053T>G	ENSP00000450392.1:p.Tyr685Asp
ENST00000551634.5:c.1960T>G	ENSP00000448373.1:p.Tyr654Asp
NM_001164749.1:c.2038T>G	NP_001158221.1:p.Tyr680Asp
NM_001165893.1:c.1948T>G	NP_001159365.1:p.Tyr650Asp
NM_022123.2:c.1942T>G	NP_071406.1:p.Tyr648Asp
NM_173159.2:c.1999T>G	NP_775182.1:p.Tyr667Asp
XM_005267991.2:c.2059T>G	XP_005268048.1:p.Tyr687Asp
XM_005267992.2:c.2053T>G	XP_005268049.1:p.Tyr685Asp
XM_005267993.2:c.1999T>G	XP_005268050.1:p.Tyr667Asp
XM_011537067.1:c.2089T>G	XP_011535369.1:p.Tyr697Asp
XM_011537068.1:c.2080T>G	XP_011535370.1:p.Tyr694Asp
XM_011537069.1:c.2050T>G	XP_011535371.1:p.Tyr684Asp
XM_011537070.1:c.1993T>G	XP_011535372.1:p.Tyr665Asp
XM_011537071.1:c.1960T>G	XP_011535373.1:p.Tyr654Asp
XM_011537072.1:c.1939T>G	XP_011535374.1:p.Tyr647Asp
XM_011537073.1:c.1732T>G	XP_011535375.1:p.Tyr578Asp
XM_011537074.1:c.1732T>G	XP_011535376.1:p.Tyr578Asp
XM_005267991.3:c.2146T>G	XP_005268048.2:p.Tyr716Asp
XM_005267992.3:c.2140T>G	XP_005268049.2:p.Tyr714Asp
XM_011537067.2:c.2089T>G	XP_011535369.1:p.Tyr697Asp
XM_011537069.2:c.2137T>G	XP_011535371.2:p.Tyr713Asp
XM_011537070.2:c.1993T>G	XP_011535372.1:p.Tyr665Asp
XM_011537071.2:c.2047T>G	XP_011535373.2:p.Tyr683Asp
XM_011537072.2:c.1939T>G	XP_011535374.1:p.Tyr647Asp
XM_017021582.1:c.2197T>G	XP_016877071.1:p.Tyr733Asp
XM_017021583.1:c.2188T>G	XP_016877072.1:p.Tyr730Asp
XM_017021584.1:c.2107T>G	XP_016877073.1:p.Tyr703Asp
XM_017021585.1:c.2056T>G	XP_016877074.1:p.Tyr686Asp
XM_017021586.1:c.1732T>G	XP_016877075.1:p.Tyr578Asp
XM_017021587.1:c.1732T>G	XP_016877076.1:p.Tyr578Asp
XM_017021588.1:c.1732T>G	XP_016877077.1:p.Tyr578Asp
NM_001164749.2:c.2038T>G MANE Select	NP_001158221.1:p.Tyr680Asp
NM_001165893.2:c.1948T>G	NP_001159365.1:p.Tyr650Asp
NM_022123.3:c.1942T>G	NP_071406.1:p.Tyr648Asp
NM_173159.3:c.1999T>G	NP_775182.1:p.Tyr667Asp
NM_001394988.1:c.1993T>G	NP_001381917.1:p.Tyr665Asp
NM_001394989.1:c.1939T>G	NP_001381918.1:p.Tyr647Asp