Canonical Allele Identifier: CA389413218

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269460G>T (hg19) ; chr14:g.33800254G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800254G>T , CM000676.2:g.33800254G>T	GRCh38
NC_000014.8:g.34269460G>T , CM000676.1:g.34269460G>T	GRCh37
NC_000014.7:g.33339211G>T	NCBI36
NG_013036.1:g.866002G>T
NG_013036.2:g.866002G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1947G>T MANE Select	ENSP00000348460.4:p.Lys649Asn
ENST00000551634.6:c.1956G>T	ENSP00000448373.2:p.Lys652Asn
ENST00000680362.1:c.1847G>T
ENST00000681323.1:c.793+2673G>T
ENST00000346562.6:c.1851G>T	ENSP00000319610.5:p.Lys617Asn
ENST00000356141.8:c.1947G>T	ENSP00000348460.4:p.Lys649Asn
ENST00000357798.9:c.1908G>T	ENSP00000350446.5:p.Lys636Asn
ENST00000548645.5:c.1857G>T	ENSP00000448916.1:p.Lys619Asn
ENST00000551492.5:c.1962G>T	ENSP00000450392.1:p.Lys654Asn
ENST00000551634.5:c.1869G>T	ENSP00000448373.1:p.Lys623Asn
NM_001164749.1:c.1947G>T	NP_001158221.1:p.Lys649Asn
NM_001165893.1:c.1857G>T	NP_001159365.1:p.Lys619Asn
NM_022123.2:c.1851G>T	NP_071406.1:p.Lys617Asn
NM_173159.2:c.1908G>T	NP_775182.1:p.Lys636Asn
XM_005267991.2:c.1968G>T	XP_005268048.1:p.Lys656Asn
XM_005267992.2:c.1962G>T	XP_005268049.1:p.Lys654Asn
XM_005267993.2:c.1908G>T	XP_005268050.1:p.Lys636Asn
XM_011537067.1:c.1998G>T	XP_011535369.1:p.Lys666Asn
XM_011537068.1:c.1989G>T	XP_011535370.1:p.Lys663Asn
XM_011537069.1:c.1959G>T	XP_011535371.1:p.Lys653Asn
XM_011537070.1:c.1902G>T	XP_011535372.1:p.Lys634Asn
XM_011537071.1:c.1869G>T	XP_011535373.1:p.Lys623Asn
XM_011537072.1:c.1848G>T	XP_011535374.1:p.Lys616Asn
XM_011537073.1:c.1641G>T	XP_011535375.1:p.Lys547Asn
XM_011537074.1:c.1641G>T	XP_011535376.1:p.Lys547Asn
XM_005267991.3:c.2055G>T	XP_005268048.2:p.Lys685Asn
XM_005267992.3:c.2049G>T	XP_005268049.2:p.Lys683Asn
XM_011537067.2:c.1998G>T	XP_011535369.1:p.Lys666Asn
XM_011537069.2:c.2046G>T	XP_011535371.2:p.Lys682Asn
XM_011537070.2:c.1902G>T	XP_011535372.1:p.Lys634Asn
XM_011537071.2:c.1956G>T	XP_011535373.2:p.Lys652Asn
XM_011537072.2:c.1848G>T	XP_011535374.1:p.Lys616Asn
XM_017021582.1:c.2106G>T	XP_016877071.1:p.Lys702Asn
XM_017021583.1:c.2097G>T	XP_016877072.1:p.Lys699Asn
XM_017021584.1:c.2016G>T	XP_016877073.1:p.Lys672Asn
XM_017021585.1:c.1965G>T	XP_016877074.1:p.Lys655Asn
XM_017021586.1:c.1641G>T	XP_016877075.1:p.Lys547Asn
XM_017021587.1:c.1641G>T	XP_016877076.1:p.Lys547Asn
XM_017021588.1:c.1641G>T	XP_016877077.1:p.Lys547Asn
NM_001164749.2:c.1947G>T MANE Select	NP_001158221.1:p.Lys649Asn
NM_001165893.2:c.1857G>T	NP_001159365.1:p.Lys619Asn
NM_022123.3:c.1851G>T	NP_071406.1:p.Lys617Asn
NM_173159.3:c.1908G>T	NP_775182.1:p.Lys636Asn
NM_001394988.1:c.1902G>T	NP_001381917.1:p.Lys634Asn
NM_001394989.1:c.1848G>T	NP_001381918.1:p.Lys616Asn