Canonical Allele Identifier: CA2838212416

Gene: NAV1 IPO9-AS1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.201718304G>C , CM000663.2:g.201718304G>C	GRCh38
NC_000001.10:g.201687432G>C , CM000663.1:g.201687432G>C	GRCh37
NC_000001.9:g.199954055G>C	NCBI36
NG_053179.1:g.74983G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685211.1:c.1722-86G>C (NAV1) MANE Select	ENSP00000510803.1:n.1722-86G>C
ENST00000367296.8:c.861-86G>C (NAV1)	ENSP00000356265.4:n.861-86G>C
ENST00000367302.5:c.900-86G>C (NAV1)	ENSP00000356271.1:n.900-86G>C
NM_020443.4:c.861-86G>C (NAV1)	NP_065176.3:n.861-86G>C
NR_046696.1:n.685-29891C>G (IPO9-AS1)
XM_011510097.1:c.861-86G>C (NAV1)	XP_011508399.1:n.861-86G>C
XM_011510098.1:c.861-86G>C (NAV1)	XP_011508400.1:n.861-86G>C
XM_011510099.1:c.861-86G>C (NAV1)	XP_011508401.1:n.861-86G>C
XM_011510100.1:c.861-86G>C (NAV1)	XP_011508402.1:n.861-86G>C
XM_011510101.1:c.861-86G>C (NAV1)	XP_011508403.1:n.861-86G>C
XM_011510102.1:c.861-86G>C (NAV1)	XP_011508404.1:n.861-86G>C
XM_011510103.1:c.930-86G>C (NAV1)	XP_011508405.1:n.930-86G>C
XR_921992.1:n.887-86G>C (NAV1)
XM_011510097.2:c.861-86G>C (NAV1)	XP_011508399.1:n.861-86G>C
XM_011510098.2:c.861-86G>C (NAV1)	XP_011508400.1:n.861-86G>C
XM_011510099.2:c.861-86G>C (NAV1)	XP_011508401.1:n.861-86G>C
XM_011510100.2:c.861-86G>C (NAV1)	XP_011508402.1:n.861-86G>C
XM_011510101.2:c.861-86G>C (NAV1)	XP_011508403.1:n.861-86G>C
XM_011510102.2:c.861-86G>C (NAV1)	XP_011508404.1:n.861-86G>C
XM_017002751.2:c.861-86G>C (NAV1)	XP_016858240.1:n.861-86G>C
XM_017002753.2:c.861-86G>C (NAV1)	XP_016858242.1:n.861-86G>C
XM_017002754.2:c.861-86G>C (NAV1)	XP_016858243.1:n.861-86G>C
XM_024450645.1:c.930-86G>C (NAV1)	XP_024306413.1:n.930-86G>C
NM_001389615.1:c.1722-86G>C (NAV1)	NP_001376544.1:n.1722-86G>C
NM_001389616.1:c.1722-86G>C (NAV1)	NP_001376545.1:n.1722-86G>C
NM_001389617.1:c.1722-86G>C (NAV1) MANE Select	NP_001376546.1:n.1722-86G>C
NM_020443.5:c.861-86G>C (NAV1)	NP_065176.3:n.861-86G>C