Canonical Allele Identifier: CA389414322

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269782G>C (hg19) ; chr14:g.33800576G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800576G>C , CM000676.2:g.33800576G>C	GRCh38
NC_000014.8:g.34269782G>C , CM000676.1:g.34269782G>C	GRCh37
NC_000014.7:g.33339533G>C	NCBI36
NG_013036.1:g.866324G>C
NG_013036.2:g.866324G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2269G>C MANE Select	ENSP00000348460.4:p.Asp757His
ENST00000551634.6:c.2278G>C	ENSP00000448373.2:p.Asp760His
ENST00000680362.1:c.2169G>C
ENST00000681323.1:c.793+2995G>C
ENST00000346562.6:c.2173G>C	ENSP00000319610.5:p.Asp725His
ENST00000356141.8:c.2269G>C	ENSP00000348460.4:p.Asp757His
ENST00000357798.9:c.2230G>C	ENSP00000350446.5:p.Asp744His
ENST00000548645.5:c.2179G>C	ENSP00000448916.1:p.Asp727His
ENST00000551492.5:c.2284G>C	ENSP00000450392.1:p.Asp762His
ENST00000551634.5:c.2191G>C	ENSP00000448373.1:p.Asp731His
NM_001164749.1:c.2269G>C	NP_001158221.1:p.Asp757His
NM_001165893.1:c.2179G>C	NP_001159365.1:p.Asp727His
NM_022123.2:c.2173G>C	NP_071406.1:p.Asp725His
NM_173159.2:c.2230G>C	NP_775182.1:p.Asp744His
XM_005267991.2:c.2290G>C	XP_005268048.1:p.Asp764His
XM_005267992.2:c.2284G>C	XP_005268049.1:p.Asp762His
XM_005267993.2:c.2230G>C	XP_005268050.1:p.Asp744His
XM_011537067.1:c.2320G>C	XP_011535369.1:p.Asp774His
XM_011537068.1:c.2311G>C	XP_011535370.1:p.Asp771His
XM_011537069.1:c.2281G>C	XP_011535371.1:p.Asp761His
XM_011537070.1:c.2224G>C	XP_011535372.1:p.Asp742His
XM_011537071.1:c.2191G>C	XP_011535373.1:p.Asp731His
XM_011537072.1:c.2170G>C	XP_011535374.1:p.Asp724His
XM_011537073.1:c.1963G>C	XP_011535375.1:p.Asp655His
XM_011537074.1:c.1963G>C	XP_011535376.1:p.Asp655His
XM_005267991.3:c.2377G>C	XP_005268048.2:p.Asp793His
XM_005267992.3:c.2371G>C	XP_005268049.2:p.Asp791His
XM_011537067.2:c.2320G>C	XP_011535369.1:p.Asp774His
XM_011537069.2:c.2368G>C	XP_011535371.2:p.Asp790His
XM_011537070.2:c.2224G>C	XP_011535372.1:p.Asp742His
XM_011537071.2:c.2278G>C	XP_011535373.2:p.Asp760His
XM_011537072.2:c.2170G>C	XP_011535374.1:p.Asp724His
XM_017021582.1:c.2428G>C	XP_016877071.1:p.Asp810His
XM_017021583.1:c.2419G>C	XP_016877072.1:p.Asp807His
XM_017021584.1:c.2338G>C	XP_016877073.1:p.Asp780His
XM_017021585.1:c.2287G>C	XP_016877074.1:p.Asp763His
XM_017021586.1:c.1963G>C	XP_016877075.1:p.Asp655His
XM_017021587.1:c.1963G>C	XP_016877076.1:p.Asp655His
XM_017021588.1:c.1963G>C	XP_016877077.1:p.Asp655His
NM_001164749.2:c.2269G>C MANE Select	NP_001158221.1:p.Asp757His
NM_001165893.2:c.2179G>C	NP_001159365.1:p.Asp727His
NM_022123.3:c.2173G>C	NP_071406.1:p.Asp725His
NM_173159.3:c.2230G>C	NP_775182.1:p.Asp744His
NM_001394988.1:c.2224G>C	NP_001381917.1:p.Asp742His
NM_001394989.1:c.2170G>C	NP_001381918.1:p.Asp724His