Canonical Allele Identifier: CA360371478

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89988527G>C (hg19) ; chr5:g.90692710G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692710G>C , CM000667.2:g.90692710G>C	GRCh38
NC_000005.9:g.89988527G>C , CM000667.1:g.89988527G>C	GRCh37
NC_000005.8:g.90024283G>C	NCBI36
NG_007083.1:g.138911G>C
NG_007083.2:g.168367G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7057G>C MANE Select	ENSP00000384582.2:p.Ala2353Pro
ENST00000639431.1:c.265+16501G>C	ENSP00000491057.1:n.265+16501G>C
ENST00000639473.1:n.2516G>C
ENST00000640012.1:c.864G>C
ENST00000640374.1:n.201G>C
ENST00000640403.1:c.4348G>C	ENSP00000492531.1:p.Ala1450Pro
ENST00000640779.1:c.1786G>C
ENST00000405460.6:c.7057G>C	ENSP00000384582.2:p.Ala2353Pro
NM_032119.3:c.7057G>C	NP_115495.3:p.Ala2353Pro
NR_003149.1:n.7070G>C
XM_011543675.1:c.7054G>C	XP_011541977.1:p.Ala2352Pro
XM_011543676.1:c.6976G>C	XP_011541978.1:p.Ala2326Pro
XM_011543677.1:c.4360G>C	XP_011541979.1:p.Ala1454Pro
XM_011543678.1:c.7057G>C	XP_011541980.1:p.Ala2353Pro
XM_011543679.1:c.7057G>C	XP_011541981.1:p.Ala2353Pro
NM_032119.4:c.7057G>C MANE Select	NP_115495.3:p.Ala2353Pro
XM_017009963.2:c.7057G>C	XP_016865452.1:p.Ala2353Pro
XM_017009964.2:c.7054G>C	XP_016865453.1:p.Ala2352Pro
XM_017009965.1:c.7054G>C	XP_016865454.1:p.Ala2352Pro
XM_017009966.2:c.6976G>C	XP_016865455.1:p.Ala2326Pro
XM_017009967.1:c.6961G>C	XP_016865456.1:p.Ala2321Pro
XM_017009968.2:c.7057G>C	XP_016865457.1:p.Ala2353Pro
XM_017009969.2:c.7057G>C	XP_016865458.1:p.Ala2353Pro
XM_017009970.2:c.7057G>C	XP_016865459.1:p.Ala2353Pro
XM_017009971.2:c.7057G>C	XP_016865460.1:p.Ala2353Pro
XM_017009972.1:c.175G>C	XP_016865461.1:p.Ala59Pro
XM_017009973.1:c.175G>C	XP_016865462.1:p.Ala59Pro
XM_017009974.2:c.7057G>C	XP_016865463.1:p.Ala2353Pro
NR_003149.2:n.7073G>C