Canonical Allele Identifier: CA389414347

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269791C>G (hg19) ; chr14:g.33800585C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800585C>G , CM000676.2:g.33800585C>G	GRCh38
NC_000014.8:g.34269791C>G , CM000676.1:g.34269791C>G	GRCh37
NC_000014.7:g.33339542C>G	NCBI36
NG_013036.1:g.866333C>G
NG_013036.2:g.866333C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2278C>G MANE Select	ENSP00000348460.4:p.Pro760Ala
ENST00000551634.6:c.2287C>G	ENSP00000448373.2:p.Pro763Ala
ENST00000680362.1:c.2178C>G
ENST00000681323.1:c.793+3004C>G
ENST00000346562.6:c.2182C>G	ENSP00000319610.5:p.Pro728Ala
ENST00000356141.8:c.2278C>G	ENSP00000348460.4:p.Pro760Ala
ENST00000357798.9:c.2239C>G	ENSP00000350446.5:p.Pro747Ala
ENST00000548645.5:c.2188C>G	ENSP00000448916.1:p.Pro730Ala
ENST00000551492.5:c.2293C>G	ENSP00000450392.1:p.Pro765Ala
ENST00000551634.5:c.2200C>G	ENSP00000448373.1:p.Pro734Ala
NM_001164749.1:c.2278C>G	NP_001158221.1:p.Pro760Ala
NM_001165893.1:c.2188C>G	NP_001159365.1:p.Pro730Ala
NM_022123.2:c.2182C>G	NP_071406.1:p.Pro728Ala
NM_173159.2:c.2239C>G	NP_775182.1:p.Pro747Ala
XM_005267991.2:c.2299C>G	XP_005268048.1:p.Pro767Ala
XM_005267992.2:c.2293C>G	XP_005268049.1:p.Pro765Ala
XM_005267993.2:c.2239C>G	XP_005268050.1:p.Pro747Ala
XM_011537067.1:c.2329C>G	XP_011535369.1:p.Pro777Ala
XM_011537068.1:c.2320C>G	XP_011535370.1:p.Pro774Ala
XM_011537069.1:c.2290C>G	XP_011535371.1:p.Pro764Ala
XM_011537070.1:c.2233C>G	XP_011535372.1:p.Pro745Ala
XM_011537071.1:c.2200C>G	XP_011535373.1:p.Pro734Ala
XM_011537072.1:c.2179C>G	XP_011535374.1:p.Pro727Ala
XM_011537073.1:c.1972C>G	XP_011535375.1:p.Pro658Ala
XM_011537074.1:c.1972C>G	XP_011535376.1:p.Pro658Ala
XM_005267991.3:c.2386C>G	XP_005268048.2:p.Pro796Ala
XM_005267992.3:c.2380C>G	XP_005268049.2:p.Pro794Ala
XM_011537067.2:c.2329C>G	XP_011535369.1:p.Pro777Ala
XM_011537069.2:c.2377C>G	XP_011535371.2:p.Pro793Ala
XM_011537070.2:c.2233C>G	XP_011535372.1:p.Pro745Ala
XM_011537071.2:c.2287C>G	XP_011535373.2:p.Pro763Ala
XM_011537072.2:c.2179C>G	XP_011535374.1:p.Pro727Ala
XM_017021582.1:c.2437C>G	XP_016877071.1:p.Pro813Ala
XM_017021583.1:c.2428C>G	XP_016877072.1:p.Pro810Ala
XM_017021584.1:c.2347C>G	XP_016877073.1:p.Pro783Ala
XM_017021585.1:c.2296C>G	XP_016877074.1:p.Pro766Ala
XM_017021586.1:c.1972C>G	XP_016877075.1:p.Pro658Ala
XM_017021587.1:c.1972C>G	XP_016877076.1:p.Pro658Ala
XM_017021588.1:c.1972C>G	XP_016877077.1:p.Pro658Ala
NM_001164749.2:c.2278C>G MANE Select	NP_001158221.1:p.Pro760Ala
NM_001165893.2:c.2188C>G	NP_001159365.1:p.Pro730Ala
NM_022123.3:c.2182C>G	NP_071406.1:p.Pro728Ala
NM_173159.3:c.2239C>G	NP_775182.1:p.Pro747Ala
NM_001394988.1:c.2233C>G	NP_001381917.1:p.Pro745Ala
NM_001394989.1:c.2179C>G	NP_001381918.1:p.Pro727Ala