Canonical Allele Identifier: CA389413358

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269491A>T (hg19) ; chr14:g.33800285A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800285A>T , CM000676.2:g.33800285A>T	GRCh38
NC_000014.8:g.34269491A>T , CM000676.1:g.34269491A>T	GRCh37
NC_000014.7:g.33339242A>T	NCBI36
NG_013036.1:g.866033A>T
NG_013036.2:g.866033A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1978A>T MANE Select	ENSP00000348460.4:p.Asn660Tyr
ENST00000551634.6:c.1987A>T	ENSP00000448373.2:p.Asn663Tyr
ENST00000680362.1:c.1878A>T
ENST00000681323.1:c.793+2704A>T
ENST00000346562.6:c.1882A>T	ENSP00000319610.5:p.Asn628Tyr
ENST00000356141.8:c.1978A>T	ENSP00000348460.4:p.Asn660Tyr
ENST00000357798.9:c.1939A>T	ENSP00000350446.5:p.Asn647Tyr
ENST00000548645.5:c.1888A>T	ENSP00000448916.1:p.Asn630Tyr
ENST00000551492.5:c.1993A>T	ENSP00000450392.1:p.Asn665Tyr
ENST00000551634.5:c.1900A>T	ENSP00000448373.1:p.Asn634Tyr
NM_001164749.1:c.1978A>T	NP_001158221.1:p.Asn660Tyr
NM_001165893.1:c.1888A>T	NP_001159365.1:p.Asn630Tyr
NM_022123.2:c.1882A>T	NP_071406.1:p.Asn628Tyr
NM_173159.2:c.1939A>T	NP_775182.1:p.Asn647Tyr
XM_005267991.2:c.1999A>T	XP_005268048.1:p.Asn667Tyr
XM_005267992.2:c.1993A>T	XP_005268049.1:p.Asn665Tyr
XM_005267993.2:c.1939A>T	XP_005268050.1:p.Asn647Tyr
XM_011537067.1:c.2029A>T	XP_011535369.1:p.Asn677Tyr
XM_011537068.1:c.2020A>T	XP_011535370.1:p.Asn674Tyr
XM_011537069.1:c.1990A>T	XP_011535371.1:p.Asn664Tyr
XM_011537070.1:c.1933A>T	XP_011535372.1:p.Asn645Tyr
XM_011537071.1:c.1900A>T	XP_011535373.1:p.Asn634Tyr
XM_011537072.1:c.1879A>T	XP_011535374.1:p.Asn627Tyr
XM_011537073.1:c.1672A>T	XP_011535375.1:p.Asn558Tyr
XM_011537074.1:c.1672A>T	XP_011535376.1:p.Asn558Tyr
XM_005267991.3:c.2086A>T	XP_005268048.2:p.Asn696Tyr
XM_005267992.3:c.2080A>T	XP_005268049.2:p.Asn694Tyr
XM_011537067.2:c.2029A>T	XP_011535369.1:p.Asn677Tyr
XM_011537069.2:c.2077A>T	XP_011535371.2:p.Asn693Tyr
XM_011537070.2:c.1933A>T	XP_011535372.1:p.Asn645Tyr
XM_011537071.2:c.1987A>T	XP_011535373.2:p.Asn663Tyr
XM_011537072.2:c.1879A>T	XP_011535374.1:p.Asn627Tyr
XM_017021582.1:c.2137A>T	XP_016877071.1:p.Asn713Tyr
XM_017021583.1:c.2128A>T	XP_016877072.1:p.Asn710Tyr
XM_017021584.1:c.2047A>T	XP_016877073.1:p.Asn683Tyr
XM_017021585.1:c.1996A>T	XP_016877074.1:p.Asn666Tyr
XM_017021586.1:c.1672A>T	XP_016877075.1:p.Asn558Tyr
XM_017021587.1:c.1672A>T	XP_016877076.1:p.Asn558Tyr
XM_017021588.1:c.1672A>T	XP_016877077.1:p.Asn558Tyr
NM_001164749.2:c.1978A>T MANE Select	NP_001158221.1:p.Asn660Tyr
NM_001165893.2:c.1888A>T	NP_001159365.1:p.Asn630Tyr
NM_022123.3:c.1882A>T	NP_071406.1:p.Asn628Tyr
NM_173159.3:c.1939A>T	NP_775182.1:p.Asn647Tyr
NM_001394988.1:c.1933A>T	NP_001381917.1:p.Asn645Tyr
NM_001394989.1:c.1879A>T	NP_001381918.1:p.Asn627Tyr