Canonical Allele Identifier: CA389413285

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269476C>G (hg19) ; chr14:g.33800270C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800270C>G , CM000676.2:g.33800270C>G	GRCh38
NC_000014.8:g.34269476C>G , CM000676.1:g.34269476C>G	GRCh37
NC_000014.7:g.33339227C>G	NCBI36
NG_013036.1:g.866018C>G
NG_013036.2:g.866018C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.1963C>G MANE Select	ENSP00000348460.4:p.Pro655Ala
ENST00000551634.6:c.1972C>G	ENSP00000448373.2:p.Pro658Ala
ENST00000680362.1:c.1863C>G
ENST00000681323.1:c.793+2689C>G
ENST00000346562.6:c.1867C>G	ENSP00000319610.5:p.Pro623Ala
ENST00000356141.8:c.1963C>G	ENSP00000348460.4:p.Pro655Ala
ENST00000357798.9:c.1924C>G	ENSP00000350446.5:p.Pro642Ala
ENST00000548645.5:c.1873C>G	ENSP00000448916.1:p.Pro625Ala
ENST00000551492.5:c.1978C>G	ENSP00000450392.1:p.Pro660Ala
ENST00000551634.5:c.1885C>G	ENSP00000448373.1:p.Pro629Ala
NM_001164749.1:c.1963C>G	NP_001158221.1:p.Pro655Ala
NM_001165893.1:c.1873C>G	NP_001159365.1:p.Pro625Ala
NM_022123.2:c.1867C>G	NP_071406.1:p.Pro623Ala
NM_173159.2:c.1924C>G	NP_775182.1:p.Pro642Ala
XM_005267991.2:c.1984C>G	XP_005268048.1:p.Pro662Ala
XM_005267992.2:c.1978C>G	XP_005268049.1:p.Pro660Ala
XM_005267993.2:c.1924C>G	XP_005268050.1:p.Pro642Ala
XM_011537067.1:c.2014C>G	XP_011535369.1:p.Pro672Ala
XM_011537068.1:c.2005C>G	XP_011535370.1:p.Pro669Ala
XM_011537069.1:c.1975C>G	XP_011535371.1:p.Pro659Ala
XM_011537070.1:c.1918C>G	XP_011535372.1:p.Pro640Ala
XM_011537071.1:c.1885C>G	XP_011535373.1:p.Pro629Ala
XM_011537072.1:c.1864C>G	XP_011535374.1:p.Pro622Ala
XM_011537073.1:c.1657C>G	XP_011535375.1:p.Pro553Ala
XM_011537074.1:c.1657C>G	XP_011535376.1:p.Pro553Ala
XM_005267991.3:c.2071C>G	XP_005268048.2:p.Pro691Ala
XM_005267992.3:c.2065C>G	XP_005268049.2:p.Pro689Ala
XM_011537067.2:c.2014C>G	XP_011535369.1:p.Pro672Ala
XM_011537069.2:c.2062C>G	XP_011535371.2:p.Pro688Ala
XM_011537070.2:c.1918C>G	XP_011535372.1:p.Pro640Ala
XM_011537071.2:c.1972C>G	XP_011535373.2:p.Pro658Ala
XM_011537072.2:c.1864C>G	XP_011535374.1:p.Pro622Ala
XM_017021582.1:c.2122C>G	XP_016877071.1:p.Pro708Ala
XM_017021583.1:c.2113C>G	XP_016877072.1:p.Pro705Ala
XM_017021584.1:c.2032C>G	XP_016877073.1:p.Pro678Ala
XM_017021585.1:c.1981C>G	XP_016877074.1:p.Pro661Ala
XM_017021586.1:c.1657C>G	XP_016877075.1:p.Pro553Ala
XM_017021587.1:c.1657C>G	XP_016877076.1:p.Pro553Ala
XM_017021588.1:c.1657C>G	XP_016877077.1:p.Pro553Ala
NM_001164749.2:c.1963C>G MANE Select	NP_001158221.1:p.Pro655Ala
NM_001165893.2:c.1873C>G	NP_001159365.1:p.Pro625Ala
NM_022123.3:c.1867C>G	NP_071406.1:p.Pro623Ala
NM_173159.3:c.1924C>G	NP_775182.1:p.Pro642Ala
NM_001394988.1:c.1918C>G	NP_001381917.1:p.Pro640Ala
NM_001394989.1:c.1864C>G	NP_001381918.1:p.Pro622Ala