Canonical Allele Identifier: CA389413480

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269516C>G (hg19) ; chr14:g.33800310C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800310C>G , CM000676.2:g.33800310C>G	GRCh38
NC_000014.8:g.34269516C>G , CM000676.1:g.34269516C>G	GRCh37
NC_000014.7:g.33339267C>G	NCBI36
NG_013036.1:g.866058C>G
NG_013036.2:g.866058C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2003C>G MANE Select	ENSP00000348460.4:p.Pro668Arg
ENST00000551634.6:c.2012C>G	ENSP00000448373.2:p.Pro671Arg
ENST00000680362.1:c.1903C>G
ENST00000681323.1:c.793+2729C>G
ENST00000346562.6:c.1907C>G	ENSP00000319610.5:p.Pro636Arg
ENST00000356141.8:c.2003C>G	ENSP00000348460.4:p.Pro668Arg
ENST00000357798.9:c.1964C>G	ENSP00000350446.5:p.Pro655Arg
ENST00000548645.5:c.1913C>G	ENSP00000448916.1:p.Pro638Arg
ENST00000551492.5:c.2018C>G	ENSP00000450392.1:p.Pro673Arg
ENST00000551634.5:c.1925C>G	ENSP00000448373.1:p.Pro642Arg
NM_001164749.1:c.2003C>G	NP_001158221.1:p.Pro668Arg
NM_001165893.1:c.1913C>G	NP_001159365.1:p.Pro638Arg
NM_022123.2:c.1907C>G	NP_071406.1:p.Pro636Arg
NM_173159.2:c.1964C>G	NP_775182.1:p.Pro655Arg
XM_005267991.2:c.2024C>G	XP_005268048.1:p.Pro675Arg
XM_005267992.2:c.2018C>G	XP_005268049.1:p.Pro673Arg
XM_005267993.2:c.1964C>G	XP_005268050.1:p.Pro655Arg
XM_011537067.1:c.2054C>G	XP_011535369.1:p.Pro685Arg
XM_011537068.1:c.2045C>G	XP_011535370.1:p.Pro682Arg
XM_011537069.1:c.2015C>G	XP_011535371.1:p.Pro672Arg
XM_011537070.1:c.1958C>G	XP_011535372.1:p.Pro653Arg
XM_011537071.1:c.1925C>G	XP_011535373.1:p.Pro642Arg
XM_011537072.1:c.1904C>G	XP_011535374.1:p.Pro635Arg
XM_011537073.1:c.1697C>G	XP_011535375.1:p.Pro566Arg
XM_011537074.1:c.1697C>G	XP_011535376.1:p.Pro566Arg
XM_005267991.3:c.2111C>G	XP_005268048.2:p.Pro704Arg
XM_005267992.3:c.2105C>G	XP_005268049.2:p.Pro702Arg
XM_011537067.2:c.2054C>G	XP_011535369.1:p.Pro685Arg
XM_011537069.2:c.2102C>G	XP_011535371.2:p.Pro701Arg
XM_011537070.2:c.1958C>G	XP_011535372.1:p.Pro653Arg
XM_011537071.2:c.2012C>G	XP_011535373.2:p.Pro671Arg
XM_011537072.2:c.1904C>G	XP_011535374.1:p.Pro635Arg
XM_017021582.1:c.2162C>G	XP_016877071.1:p.Pro721Arg
XM_017021583.1:c.2153C>G	XP_016877072.1:p.Pro718Arg
XM_017021584.1:c.2072C>G	XP_016877073.1:p.Pro691Arg
XM_017021585.1:c.2021C>G	XP_016877074.1:p.Pro674Arg
XM_017021586.1:c.1697C>G	XP_016877075.1:p.Pro566Arg
XM_017021587.1:c.1697C>G	XP_016877076.1:p.Pro566Arg
XM_017021588.1:c.1697C>G	XP_016877077.1:p.Pro566Arg
NM_001164749.2:c.2003C>G MANE Select	NP_001158221.1:p.Pro668Arg
NM_001165893.2:c.1913C>G	NP_001159365.1:p.Pro638Arg
NM_022123.3:c.1907C>G	NP_071406.1:p.Pro636Arg
NM_173159.3:c.1964C>G	NP_775182.1:p.Pro655Arg
NM_001394988.1:c.1958C>G	NP_001381917.1:p.Pro653Arg
NM_001394989.1:c.1904C>G	NP_001381918.1:p.Pro635Arg