Canonical Allele Identifier: CA730119689

Gene: NAV1

Linked Data

• dbSNP Id: rs586688
• MyVariant Identifiers: chr1:g.201630955G>T (hg19) ; chr1:g.201661827G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201661827G>T , CM000663.2:g.201661827G>T	GRCh38
NC_000001.10:g.201630955G>T , CM000663.1:g.201630955G>T	GRCh37
NC_000001.9:g.199897578G>T	NCBI36
NG_053179.1:g.18506G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000685211.1:c.1618+12402G>T MANE Select	ENSP00000510803.1:n.1618+12402G>T
ENST00000367296.8:c.757+12402G>T	ENSP00000356265.4:n.757+12402G>T
ENST00000367302.5:c.796+12402G>T	ENSP00000356271.1:n.796+12402G>T
NM_020443.4:c.757+12402G>T	NP_065176.3:n.757+12402G>T
XM_011510097.1:c.757+12402G>T	XP_011508399.1:n.757+12402G>T
XM_011510098.1:c.757+12402G>T	XP_011508400.1:n.757+12402G>T
XM_011510099.1:c.757+12402G>T	XP_011508401.1:n.757+12402G>T
XM_011510100.1:c.757+12402G>T	XP_011508402.1:n.757+12402G>T
XM_011510101.1:c.757+12402G>T	XP_011508403.1:n.757+12402G>T
XM_011510102.1:c.757+12402G>T	XP_011508404.1:n.757+12402G>T
XM_011510103.1:c.826+32320G>T	XP_011508405.1:n.826+32320G>T
XR_921992.1:n.783+12402G>T
XM_011510097.2:c.757+12402G>T	XP_011508399.1:n.757+12402G>T
XM_011510098.2:c.757+12402G>T	XP_011508400.1:n.757+12402G>T
XM_011510099.2:c.757+12402G>T	XP_011508401.1:n.757+12402G>T
XM_011510100.2:c.757+12402G>T	XP_011508402.1:n.757+12402G>T
XM_011510101.2:c.757+12402G>T	XP_011508403.1:n.757+12402G>T
XM_011510102.2:c.757+12402G>T	XP_011508404.1:n.757+12402G>T
XM_017002751.2:c.757+12402G>T	XP_016858240.1:n.757+12402G>T
XM_017002753.2:c.757+12402G>T	XP_016858242.1:n.757+12402G>T
XM_017002754.2:c.757+12402G>T	XP_016858243.1:n.757+12402G>T
XM_024450645.1:c.826+32320G>T	XP_024306413.1:n.826+32320G>T
NM_001389615.1:c.1618+12402G>T	NP_001376544.1:n.1618+12402G>T
NM_001389616.1:c.1618+12402G>T	NP_001376545.1:n.1618+12402G>T
NM_001389617.1:c.1618+12402G>T MANE Select	NP_001376546.1:n.1618+12402G>T
NM_020443.5:c.757+12402G>T	NP_065176.3:n.757+12402G>T