Canonical Allele Identifier: CA389412473

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269310G>T (hg19) ; chr14:g.33800104G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800104G>T , CM000676.2:g.33800104G>T	GRCh38
NC_000014.8:g.34269310G>T , CM000676.1:g.34269310G>T	GRCh37
NC_000014.7:g.33339061G>T	NCBI36
NG_013036.1:g.865852G>T
NG_013036.2:g.865852G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1797G>T MANE Select	ENSP00000348460.4:p.Lys599Asn
ENST00000551634.6:c.1806G>T	ENSP00000448373.2:p.Lys602Asn
ENST00000680362.1:c.1697G>T
ENST00000681323.1:c.793+2523G>T
ENST00000346562.6:c.1701G>T	ENSP00000319610.5:p.Lys567Asn
ENST00000356141.8:c.1797G>T	ENSP00000348460.4:p.Lys599Asn
ENST00000357798.9:c.1758G>T	ENSP00000350446.5:p.Lys586Asn
ENST00000548645.5:c.1707G>T	ENSP00000448916.1:p.Lys569Asn
ENST00000551492.5:c.1812G>T	ENSP00000450392.1:p.Lys604Asn
ENST00000551634.5:c.1719G>T	ENSP00000448373.1:p.Lys573Asn
NM_001164749.1:c.1797G>T	NP_001158221.1:p.Lys599Asn
NM_001165893.1:c.1707G>T	NP_001159365.1:p.Lys569Asn
NM_022123.2:c.1701G>T	NP_071406.1:p.Lys567Asn
NM_173159.2:c.1758G>T	NP_775182.1:p.Lys586Asn
XM_005267991.2:c.1818G>T	XP_005268048.1:p.Lys606Asn
XM_005267992.2:c.1812G>T	XP_005268049.1:p.Lys604Asn
XM_005267993.2:c.1758G>T	XP_005268050.1:p.Lys586Asn
XM_011537067.1:c.1848G>T	XP_011535369.1:p.Lys616Asn
XM_011537068.1:c.1839G>T	XP_011535370.1:p.Lys613Asn
XM_011537069.1:c.1809G>T	XP_011535371.1:p.Lys603Asn
XM_011537070.1:c.1752G>T	XP_011535372.1:p.Lys584Asn
XM_011537071.1:c.1719G>T	XP_011535373.1:p.Lys573Asn
XM_011537072.1:c.1698G>T	XP_011535374.1:p.Lys566Asn
XM_011537073.1:c.1491G>T	XP_011535375.1:p.Lys497Asn
XM_011537074.1:c.1491G>T	XP_011535376.1:p.Lys497Asn
XM_005267991.3:c.1905G>T	XP_005268048.2:p.Lys635Asn
XM_005267992.3:c.1899G>T	XP_005268049.2:p.Lys633Asn
XM_011537067.2:c.1848G>T	XP_011535369.1:p.Lys616Asn
XM_011537069.2:c.1896G>T	XP_011535371.2:p.Lys632Asn
XM_011537070.2:c.1752G>T	XP_011535372.1:p.Lys584Asn
XM_011537071.2:c.1806G>T	XP_011535373.2:p.Lys602Asn
XM_011537072.2:c.1698G>T	XP_011535374.1:p.Lys566Asn
XM_017021582.1:c.1956G>T	XP_016877071.1:p.Lys652Asn
XM_017021583.1:c.1947G>T	XP_016877072.1:p.Lys649Asn
XM_017021584.1:c.1866G>T	XP_016877073.1:p.Lys622Asn
XM_017021585.1:c.1815G>T	XP_016877074.1:p.Lys605Asn
XM_017021586.1:c.1491G>T	XP_016877075.1:p.Lys497Asn
XM_017021587.1:c.1491G>T	XP_016877076.1:p.Lys497Asn
XM_017021588.1:c.1491G>T	XP_016877077.1:p.Lys497Asn
NM_001164749.2:c.1797G>T MANE Select	NP_001158221.1:p.Lys599Asn
NM_001165893.2:c.1707G>T	NP_001159365.1:p.Lys569Asn
NM_022123.3:c.1701G>T	NP_071406.1:p.Lys567Asn
NM_173159.3:c.1758G>T	NP_775182.1:p.Lys586Asn
NM_001394988.1:c.1752G>T	NP_001381917.1:p.Lys584Asn
NM_001394989.1:c.1698G>T	NP_001381918.1:p.Lys566Asn