Canonical Allele Identifier: CA389413342

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269488G>C (hg19) ; chr14:g.33800282G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800282G>C , CM000676.2:g.33800282G>C	GRCh38
NC_000014.8:g.34269488G>C , CM000676.1:g.34269488G>C	GRCh37
NC_000014.7:g.33339239G>C	NCBI36
NG_013036.1:g.866030G>C
NG_013036.2:g.866030G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1975G>C MANE Select	ENSP00000348460.4:p.Asp659His
ENST00000551634.6:c.1984G>C	ENSP00000448373.2:p.Asp662His
ENST00000680362.1:c.1875G>C
ENST00000681323.1:c.793+2701G>C
ENST00000346562.6:c.1879G>C	ENSP00000319610.5:p.Asp627His
ENST00000356141.8:c.1975G>C	ENSP00000348460.4:p.Asp659His
ENST00000357798.9:c.1936G>C	ENSP00000350446.5:p.Asp646His
ENST00000548645.5:c.1885G>C	ENSP00000448916.1:p.Asp629His
ENST00000551492.5:c.1990G>C	ENSP00000450392.1:p.Asp664His
ENST00000551634.5:c.1897G>C	ENSP00000448373.1:p.Asp633His
NM_001164749.1:c.1975G>C	NP_001158221.1:p.Asp659His
NM_001165893.1:c.1885G>C	NP_001159365.1:p.Asp629His
NM_022123.2:c.1879G>C	NP_071406.1:p.Asp627His
NM_173159.2:c.1936G>C	NP_775182.1:p.Asp646His
XM_005267991.2:c.1996G>C	XP_005268048.1:p.Asp666His
XM_005267992.2:c.1990G>C	XP_005268049.1:p.Asp664His
XM_005267993.2:c.1936G>C	XP_005268050.1:p.Asp646His
XM_011537067.1:c.2026G>C	XP_011535369.1:p.Asp676His
XM_011537068.1:c.2017G>C	XP_011535370.1:p.Asp673His
XM_011537069.1:c.1987G>C	XP_011535371.1:p.Asp663His
XM_011537070.1:c.1930G>C	XP_011535372.1:p.Asp644His
XM_011537071.1:c.1897G>C	XP_011535373.1:p.Asp633His
XM_011537072.1:c.1876G>C	XP_011535374.1:p.Asp626His
XM_011537073.1:c.1669G>C	XP_011535375.1:p.Asp557His
XM_011537074.1:c.1669G>C	XP_011535376.1:p.Asp557His
XM_005267991.3:c.2083G>C	XP_005268048.2:p.Asp695His
XM_005267992.3:c.2077G>C	XP_005268049.2:p.Asp693His
XM_011537067.2:c.2026G>C	XP_011535369.1:p.Asp676His
XM_011537069.2:c.2074G>C	XP_011535371.2:p.Asp692His
XM_011537070.2:c.1930G>C	XP_011535372.1:p.Asp644His
XM_011537071.2:c.1984G>C	XP_011535373.2:p.Asp662His
XM_011537072.2:c.1876G>C	XP_011535374.1:p.Asp626His
XM_017021582.1:c.2134G>C	XP_016877071.1:p.Asp712His
XM_017021583.1:c.2125G>C	XP_016877072.1:p.Asp709His
XM_017021584.1:c.2044G>C	XP_016877073.1:p.Asp682His
XM_017021585.1:c.1993G>C	XP_016877074.1:p.Asp665His
XM_017021586.1:c.1669G>C	XP_016877075.1:p.Asp557His
XM_017021587.1:c.1669G>C	XP_016877076.1:p.Asp557His
XM_017021588.1:c.1669G>C	XP_016877077.1:p.Asp557His
NM_001164749.2:c.1975G>C MANE Select	NP_001158221.1:p.Asp659His
NM_001165893.2:c.1885G>C	NP_001159365.1:p.Asp629His
NM_022123.3:c.1879G>C	NP_071406.1:p.Asp627His
NM_173159.3:c.1936G>C	NP_775182.1:p.Asp646His
NM_001394988.1:c.1930G>C	NP_001381917.1:p.Asp644His
NM_001394989.1:c.1876G>C	NP_001381918.1:p.Asp626His