Canonical Allele Identifier: CA389413668

Gene: NPAS3

Linked Data

• MyVariant Identifiers: chr14:g.34269558T>C (hg19) ; chr14:g.33800352T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.33800352T>C , CM000676.2:g.33800352T>C	GRCh38
NC_000014.8:g.34269558T>C , CM000676.1:g.34269558T>C	GRCh37
NC_000014.7:g.33339309T>C	NCBI36
NG_013036.1:g.866100T>C
NG_013036.2:g.866100T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356141.9:c.2045T>C MANE Select	ENSP00000348460.4:p.Met682Thr
ENST00000551634.6:c.2054T>C	ENSP00000448373.2:p.Met685Thr
ENST00000680362.1:c.1945T>C
ENST00000681323.1:c.793+2771T>C
ENST00000346562.6:c.1949T>C	ENSP00000319610.5:p.Met650Thr
ENST00000356141.8:c.2045T>C	ENSP00000348460.4:p.Met682Thr
ENST00000357798.9:c.2006T>C	ENSP00000350446.5:p.Met669Thr
ENST00000548645.5:c.1955T>C	ENSP00000448916.1:p.Met652Thr
ENST00000551492.5:c.2060T>C	ENSP00000450392.1:p.Met687Thr
ENST00000551634.5:c.1967T>C	ENSP00000448373.1:p.Met656Thr
NM_001164749.1:c.2045T>C	NP_001158221.1:p.Met682Thr
NM_001165893.1:c.1955T>C	NP_001159365.1:p.Met652Thr
NM_022123.2:c.1949T>C	NP_071406.1:p.Met650Thr
NM_173159.2:c.2006T>C	NP_775182.1:p.Met669Thr
XM_005267991.2:c.2066T>C	XP_005268048.1:p.Met689Thr
XM_005267992.2:c.2060T>C	XP_005268049.1:p.Met687Thr
XM_005267993.2:c.2006T>C	XP_005268050.1:p.Met669Thr
XM_011537067.1:c.2096T>C	XP_011535369.1:p.Met699Thr
XM_011537068.1:c.2087T>C	XP_011535370.1:p.Met696Thr
XM_011537069.1:c.2057T>C	XP_011535371.1:p.Met686Thr
XM_011537070.1:c.2000T>C	XP_011535372.1:p.Met667Thr
XM_011537071.1:c.1967T>C	XP_011535373.1:p.Met656Thr
XM_011537072.1:c.1946T>C	XP_011535374.1:p.Met649Thr
XM_011537073.1:c.1739T>C	XP_011535375.1:p.Met580Thr
XM_011537074.1:c.1739T>C	XP_011535376.1:p.Met580Thr
XM_005267991.3:c.2153T>C	XP_005268048.2:p.Met718Thr
XM_005267992.3:c.2147T>C	XP_005268049.2:p.Met716Thr
XM_011537067.2:c.2096T>C	XP_011535369.1:p.Met699Thr
XM_011537069.2:c.2144T>C	XP_011535371.2:p.Met715Thr
XM_011537070.2:c.2000T>C	XP_011535372.1:p.Met667Thr
XM_011537071.2:c.2054T>C	XP_011535373.2:p.Met685Thr
XM_011537072.2:c.1946T>C	XP_011535374.1:p.Met649Thr
XM_017021582.1:c.2204T>C	XP_016877071.1:p.Met735Thr
XM_017021583.1:c.2195T>C	XP_016877072.1:p.Met732Thr
XM_017021584.1:c.2114T>C	XP_016877073.1:p.Met705Thr
XM_017021585.1:c.2063T>C	XP_016877074.1:p.Met688Thr
XM_017021586.1:c.1739T>C	XP_016877075.1:p.Met580Thr
XM_017021587.1:c.1739T>C	XP_016877076.1:p.Met580Thr
XM_017021588.1:c.1739T>C	XP_016877077.1:p.Met580Thr
NM_001164749.2:c.2045T>C MANE Select	NP_001158221.1:p.Met682Thr
NM_001165893.2:c.1955T>C	NP_001159365.1:p.Met652Thr
NM_022123.3:c.1949T>C	NP_071406.1:p.Met650Thr
NM_173159.3:c.2006T>C	NP_775182.1:p.Met669Thr
NM_001394988.1:c.2000T>C	NP_001381917.1:p.Met667Thr
NM_001394989.1:c.1946T>C	NP_001381918.1:p.Met649Thr