Canonical Allele Identifier: CA486093455

Gene: NPAS3

Linked Data

• dbSNP Id: rs2138692279
• gnomAD v3: 14-33800590-G-A
• gnomAD v4: 14-33800590-G-A
• MyVariant Identifiers: chr14:g.34269796G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800590G>A , CM000676.2:g.33800590G>A	GRCh38
NC_000014.8:g.34269796G>A , CM000676.1:g.34269796G>A	GRCh37
NC_000014.7:g.33339547G>A	NCBI36
NG_013036.1:g.866338G>A
NG_013036.2:g.866338G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000356141.9:c.2283G>A MANE Select	ENSP00000348460.4:p.Gly761=
ENST00000551634.6:c.2292G>A	ENSP00000448373.2:p.Gly764=
ENST00000680362.1:c.2183G>A
ENST00000681323.1:c.793+3009G>A
ENST00000346562.6:c.2187G>A	ENSP00000319610.5:p.Gly729=
ENST00000356141.8:c.2283G>A	ENSP00000348460.4:p.Gly761=
ENST00000357798.9:c.2244G>A	ENSP00000350446.5:p.Gly748=
ENST00000548645.5:c.2193G>A	ENSP00000448916.1:p.Gly731=
ENST00000551492.5:c.2298G>A	ENSP00000450392.1:p.Gly766=
ENST00000551634.5:c.2205G>A	ENSP00000448373.1:p.Gly735=
NM_001164749.1:c.2283G>A	NP_001158221.1:p.Gly761=
NM_001165893.1:c.2193G>A	NP_001159365.1:p.Gly731=
NM_022123.2:c.2187G>A	NP_071406.1:p.Gly729=
NM_173159.2:c.2244G>A	NP_775182.1:p.Gly748=
XM_005267991.2:c.2304G>A	XP_005268048.1:p.Gly768=
XM_005267992.2:c.2298G>A	XP_005268049.1:p.Gly766=
XM_005267993.2:c.2244G>A	XP_005268050.1:p.Gly748=
XM_011537067.1:c.2334G>A	XP_011535369.1:p.Gly778=
XM_011537068.1:c.2325G>A	XP_011535370.1:p.Gly775=
XM_011537069.1:c.2295G>A	XP_011535371.1:p.Gly765=
XM_011537070.1:c.2238G>A	XP_011535372.1:p.Gly746=
XM_011537071.1:c.2205G>A	XP_011535373.1:p.Gly735=
XM_011537072.1:c.2184G>A	XP_011535374.1:p.Gly728=
XM_011537073.1:c.1977G>A	XP_011535375.1:p.Gly659=
XM_011537074.1:c.1977G>A	XP_011535376.1:p.Gly659=
XM_005267991.3:c.2391G>A	XP_005268048.2:p.Gly797=
XM_005267992.3:c.2385G>A	XP_005268049.2:p.Gly795=
XM_011537067.2:c.2334G>A	XP_011535369.1:p.Gly778=
XM_011537069.2:c.2382G>A	XP_011535371.2:p.Gly794=
XM_011537070.2:c.2238G>A	XP_011535372.1:p.Gly746=
XM_011537071.2:c.2292G>A	XP_011535373.2:p.Gly764=
XM_011537072.2:c.2184G>A	XP_011535374.1:p.Gly728=
XM_017021582.1:c.2442G>A	XP_016877071.1:p.Gly814=
XM_017021583.1:c.2433G>A	XP_016877072.1:p.Gly811=
XM_017021584.1:c.2352G>A	XP_016877073.1:p.Gly784=
XM_017021585.1:c.2301G>A	XP_016877074.1:p.Gly767=
XM_017021586.1:c.1977G>A	XP_016877075.1:p.Gly659=
XM_017021587.1:c.1977G>A	XP_016877076.1:p.Gly659=
XM_017021588.1:c.1977G>A	XP_016877077.1:p.Gly659=
NM_001164749.2:c.2283G>A MANE Select	NP_001158221.1:p.Gly761=
NM_001165893.2:c.2193G>A	NP_001159365.1:p.Gly731=
NM_022123.3:c.2187G>A	NP_071406.1:p.Gly729=
NM_173159.3:c.2244G>A	NP_775182.1:p.Gly748=
NM_001394988.1:c.2238G>A	NP_001381917.1:p.Gly746=
NM_001394989.1:c.2184G>A	NP_001381918.1:p.Gly728=