Canonical Allele Identifier: CA389413362

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269492A>C (hg19) ; chr14:g.33800286A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800286A>C , CM000676.2:g.33800286A>C	GRCh38
NC_000014.8:g.34269492A>C , CM000676.1:g.34269492A>C	GRCh37
NC_000014.7:g.33339243A>C	NCBI36
NG_013036.1:g.866034A>C
NG_013036.2:g.866034A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1979A>C MANE Select	ENSP00000348460.4:p.Asn660Thr
ENST00000551634.6:c.1988A>C	ENSP00000448373.2:p.Asn663Thr
ENST00000680362.1:c.1879A>C
ENST00000681323.1:c.793+2705A>C
ENST00000346562.6:c.1883A>C	ENSP00000319610.5:p.Asn628Thr
ENST00000356141.8:c.1979A>C	ENSP00000348460.4:p.Asn660Thr
ENST00000357798.9:c.1940A>C	ENSP00000350446.5:p.Asn647Thr
ENST00000548645.5:c.1889A>C	ENSP00000448916.1:p.Asn630Thr
ENST00000551492.5:c.1994A>C	ENSP00000450392.1:p.Asn665Thr
ENST00000551634.5:c.1901A>C	ENSP00000448373.1:p.Asn634Thr
NM_001164749.1:c.1979A>C	NP_001158221.1:p.Asn660Thr
NM_001165893.1:c.1889A>C	NP_001159365.1:p.Asn630Thr
NM_022123.2:c.1883A>C	NP_071406.1:p.Asn628Thr
NM_173159.2:c.1940A>C	NP_775182.1:p.Asn647Thr
XM_005267991.2:c.2000A>C	XP_005268048.1:p.Asn667Thr
XM_005267992.2:c.1994A>C	XP_005268049.1:p.Asn665Thr
XM_005267993.2:c.1940A>C	XP_005268050.1:p.Asn647Thr
XM_011537067.1:c.2030A>C	XP_011535369.1:p.Asn677Thr
XM_011537068.1:c.2021A>C	XP_011535370.1:p.Asn674Thr
XM_011537069.1:c.1991A>C	XP_011535371.1:p.Asn664Thr
XM_011537070.1:c.1934A>C	XP_011535372.1:p.Asn645Thr
XM_011537071.1:c.1901A>C	XP_011535373.1:p.Asn634Thr
XM_011537072.1:c.1880A>C	XP_011535374.1:p.Asn627Thr
XM_011537073.1:c.1673A>C	XP_011535375.1:p.Asn558Thr
XM_011537074.1:c.1673A>C	XP_011535376.1:p.Asn558Thr
XM_005267991.3:c.2087A>C	XP_005268048.2:p.Asn696Thr
XM_005267992.3:c.2081A>C	XP_005268049.2:p.Asn694Thr
XM_011537067.2:c.2030A>C	XP_011535369.1:p.Asn677Thr
XM_011537069.2:c.2078A>C	XP_011535371.2:p.Asn693Thr
XM_011537070.2:c.1934A>C	XP_011535372.1:p.Asn645Thr
XM_011537071.2:c.1988A>C	XP_011535373.2:p.Asn663Thr
XM_011537072.2:c.1880A>C	XP_011535374.1:p.Asn627Thr
XM_017021582.1:c.2138A>C	XP_016877071.1:p.Asn713Thr
XM_017021583.1:c.2129A>C	XP_016877072.1:p.Asn710Thr
XM_017021584.1:c.2048A>C	XP_016877073.1:p.Asn683Thr
XM_017021585.1:c.1997A>C	XP_016877074.1:p.Asn666Thr
XM_017021586.1:c.1673A>C	XP_016877075.1:p.Asn558Thr
XM_017021587.1:c.1673A>C	XP_016877076.1:p.Asn558Thr
XM_017021588.1:c.1673A>C	XP_016877077.1:p.Asn558Thr
NM_001164749.2:c.1979A>C MANE Select	NP_001158221.1:p.Asn660Thr
NM_001165893.2:c.1889A>C	NP_001159365.1:p.Asn630Thr
NM_022123.3:c.1883A>C	NP_071406.1:p.Asn628Thr
NM_173159.3:c.1940A>C	NP_775182.1:p.Asn647Thr
NM_001394988.1:c.1934A>C	NP_001381917.1:p.Asn645Thr
NM_001394989.1:c.1880A>C	NP_001381918.1:p.Asn627Thr