Canonical Allele Identifier: CA1956356807

Gene: NAV2

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.20068432A>T , CM000673.2:g.20068432A>T	GRCh38
NC_000011.9:g.20089978A>T , CM000673.1:g.20089978A>T	GRCh37
NC_000011.8:g.20046554A>T	NCBI36
NG_030347.1:g.722708A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349880.9:c.4983+34A>T MANE Select	ENSP00000309577.6:n.4983+34A>T
ENST00000396085.6:c.4983+34A>T	ENSP00000379394.1:n.4983+34A>T
ENST00000349880.8:c.4983+34A>T	ENSP00000309577.6:n.4983+34A>T
ENST00000360655.8:c.4791+34A>T	ENSP00000353871.4:n.4791+34A>T
ENST00000396085.5:c.4983+34A>T	ENSP00000379394.1:n.4983+34A>T
ENST00000396087.7:c.5151+34A>T	ENSP00000379396.3:n.5151+34A>T
ENST00000525322.5:c.2130+34A>T	ENSP00000437136.1:n.2130+34A>T
ENST00000527559.6:c.5151+34A>T	ENSP00000435395.3:n.5151+34A>T
ENST00000533917.5:c.2175+34A>T	ENSP00000437316.1:n.2175+34A>T
ENST00000540292.5:c.4983+34A>T	ENSP00000443489.2:n.4983+34A>T
NM_001111018.1:c.4791+34A>T	NP_001104488.1:n.4791+34A>T
NM_001111019.2:c.2175+34A>T	NP_001104489.1:n.2175+34A>T
NM_001244963.1:c.5151+34A>T	NP_001231892.1:n.5151+34A>T
NM_145117.4:c.4983+34A>T	NP_660093.2:n.4983+34A>T
NM_182964.5:c.4983+34A>T	NP_892009.3:n.4983+34A>T
XM_005253214.3:c.2130+34A>T	XP_005253271.1:n.2130+34A>T
XM_006718364.2:c.5082+34A>T	XP_006718427.1:n.5082+34A>T
XM_006718365.2:c.5052+34A>T	XP_006718428.1:n.5052+34A>T
XM_006718366.2:c.4935+34A>T	XP_006718429.1:n.4935+34A>T
XM_006718367.2:c.2340+34A>T	XP_006718430.1:n.2340+34A>T
XM_006718368.2:c.2175+34A>T	XP_006718431.1:n.2175+34A>T
XM_006718369.1:c.2079+34A>T	XP_006718432.1:n.2079+34A>T
XM_011520444.1:c.5151+34A>T	XP_011518746.1:n.5151+34A>T
XM_011520445.1:c.5085+34A>T	XP_011518747.1:n.5085+34A>T
XM_011520446.1:c.5052+34A>T	XP_011518748.1:n.5052+34A>T
XM_011520447.1:c.5040+34A>T	XP_011518749.1:n.5040+34A>T
XM_011520448.1:c.5022+34A>T	XP_011518750.1:n.5022+34A>T
XM_011520449.1:c.4986+34A>T	XP_011518751.1:n.4986+34A>T
XM_011520450.1:c.4941+34A>T	XP_011518752.1:n.4941+34A>T
XM_011520451.1:c.4872+34A>T	XP_011518753.1:n.4872+34A>T
XM_011520452.1:c.4791+34A>T	XP_011518754.1:n.4791+34A>T
XM_011520453.1:c.2079+34A>T	XP_011518755.1:n.2079+34A>T
XM_011520454.1:c.1869+34A>T	XP_011518756.1:n.1869+34A>T
XM_005253214.4:c.2130+34A>T	XP_005253271.1:n.2130+34A>T
XM_006718364.4:c.5082+34A>T	XP_006718427.1:n.5082+34A>T
XM_006718365.4:c.5052+34A>T	XP_006718428.1:n.5052+34A>T
XM_006718366.4:c.4935+34A>T	XP_006718429.1:n.4935+34A>T
XM_006718367.3:c.2340+34A>T	XP_006718430.1:n.2340+34A>T
XM_006718368.3:c.2175+34A>T	XP_006718431.1:n.2175+34A>T
XM_006718369.2:c.2079+34A>T	XP_006718432.1:n.2079+34A>T
XM_011520444.3:c.5151+34A>T	XP_011518746.1:n.5151+34A>T
XM_011520445.3:c.5085+34A>T	XP_011518747.1:n.5085+34A>T
XM_011520446.3:c.5052+34A>T	XP_011518748.1:n.5052+34A>T
XM_011520447.3:c.5040+34A>T	XP_011518749.1:n.5040+34A>T
XM_011520448.3:c.5022+34A>T	XP_011518750.1:n.5022+34A>T
XM_011520449.3:c.4986+34A>T	XP_011518751.1:n.4986+34A>T
XM_011520450.3:c.4941+34A>T	XP_011518752.1:n.4941+34A>T
XM_011520451.2:c.4872+34A>T	XP_011518753.1:n.4872+34A>T
XM_011520452.2:c.4791+34A>T	XP_011518754.1:n.4791+34A>T
XM_011520453.2:c.2079+34A>T	XP_011518755.1:n.2079+34A>T
XM_011520454.2:c.1869+34A>T	XP_011518756.1:n.1869+34A>T
XM_017018520.2:c.4959+34A>T	XP_016874009.1:n.4959+34A>T
XM_017018521.2:c.4941+34A>T	XP_016874010.1:n.4941+34A>T
XM_017018522.1:c.4890+34A>T	XP_016874011.1:n.4890+34A>T
XM_017018523.1:c.4716+34A>T	XP_016874012.1:n.4716+34A>T
XM_017018524.2:c.4716+34A>T	XP_016874013.1:n.4716+34A>T
XM_017018525.1:c.4116+34A>T	XP_016874014.1:n.4116+34A>T
XM_017018526.1:c.2433+34A>T	XP_016874015.1:n.2433+34A>T
XM_024448758.1:c.4959+34A>T	XP_024304526.1:n.4959+34A>T
NM_182964.6:c.4983+34A>T	NP_892009.3:n.4983+34A>T
NM_001111019.3:c.2175+34A>T	NP_001104489.1:n.2175+34A>T
NM_001244963.2:c.5151+34A>T	NP_001231892.1:n.5151+34A>T
NM_145117.5:c.4983+34A>T MANE Select	NP_660093.2:n.4983+34A>T
NM_001111018.2:c.4791+34A>T	NP_001104488.1:n.4791+34A>T