Canonical Allele Identifier: CA5918161

Gene: NAV2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.19948955T>C , CM000673.2:g.19948955T>C	GRCh38
NC_000011.9:g.19970501T>C , CM000673.1:g.19970501T>C	GRCh37
NC_000011.8:g.19927077T>C	NCBI36
NG_030347.1:g.603231T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000349880.9:c.2520T>C MANE Select	ENSP00000309577.6:p.His840=
ENST00000396085.6:c.2520T>C	ENSP00000379394.1:p.His840=
ENST00000349880.8:c.2520T>C	ENSP00000309577.6:p.His840=
ENST00000360655.8:c.2328T>C	ENSP00000353871.4:p.His776=
ENST00000396085.5:c.2520T>C	ENSP00000379394.1:p.His840=
ENST00000396087.7:c.2589T>C	ENSP00000379396.3:p.His863=
ENST00000527559.6:c.2589T>C	ENSP00000435395.3:p.His863=
ENST00000540292.5:c.2520T>C	ENSP00000443489.2:p.His840=
NM_001111018.1:c.2328T>C	NP_001104488.1:p.His776=
NM_001244963.1:c.2589T>C	NP_001231892.1:p.His863=
NM_145117.4:c.2520T>C	NP_660093.2:p.His840=
NM_182964.5:c.2520T>C	NP_892009.3:p.His840=
XM_006718364.2:c.2520T>C	XP_006718427.1:p.His840=
XM_006718365.2:c.2589T>C	XP_006718428.1:p.His863=
XM_006718366.2:c.2373T>C	XP_006718429.1:p.His791=
XM_011520444.1:c.2589T>C	XP_011518746.1:p.His863=
XM_011520445.1:c.2589T>C	XP_011518747.1:p.His863=
XM_011520446.1:c.2589T>C	XP_011518748.1:p.His863=
XM_011520447.1:c.2589T>C	XP_011518749.1:p.His863=
XM_011520448.1:c.2460T>C	XP_011518750.1:p.His820=
XM_011520449.1:c.2589T>C	XP_011518751.1:p.His863=
XM_011520450.1:c.2589T>C	XP_011518752.1:p.His863=
XM_011520451.1:c.2310T>C	XP_011518753.1:p.His770=
XM_011520452.1:c.2328T>C	XP_011518754.1:p.His776=
XM_006718364.4:c.2520T>C	XP_006718427.1:p.His840=
XM_006718365.4:c.2589T>C	XP_006718428.1:p.His863=
XM_006718366.4:c.2373T>C	XP_006718429.1:p.His791=
XM_011520444.3:c.2589T>C	XP_011518746.1:p.His863=
XM_011520445.3:c.2589T>C	XP_011518747.1:p.His863=
XM_011520446.3:c.2589T>C	XP_011518748.1:p.His863=
XM_011520447.3:c.2589T>C	XP_011518749.1:p.His863=
XM_011520448.3:c.2460T>C	XP_011518750.1:p.His820=
XM_011520449.3:c.2589T>C	XP_011518751.1:p.His863=
XM_011520450.3:c.2589T>C	XP_011518752.1:p.His863=
XM_011520451.2:c.2310T>C	XP_011518753.1:p.His770=
XM_011520452.2:c.2328T>C	XP_011518754.1:p.His776=
XM_017018520.2:c.2397T>C	XP_016874009.1:p.His799=
XM_017018521.2:c.2589T>C	XP_016874010.1:p.His863=
XM_017018522.1:c.2328T>C	XP_016874011.1:p.His776=
XM_017018523.1:c.2154T>C	XP_016874012.1:p.His718=
XM_017018524.2:c.2154T>C	XP_016874013.1:p.His718=
XM_017018525.1:c.1554T>C	XP_016874014.1:p.His518=
XM_024448758.1:c.2397T>C	XP_024304526.1:p.His799=
NM_182964.6:c.2520T>C	NP_892009.3:p.His840=
NM_001244963.2:c.2589T>C	NP_001231892.1:p.His863=
NM_145117.5:c.2520T>C MANE Select	NP_660093.2:p.His840=
NM_001111018.2:c.2328T>C	NP_001104488.1:p.His776=