Canonical Allele Identifier: CA360396112

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90712287-A-G
• MyVariant Identifiers: chr5:g.90008104A>G (hg19) ; chr5:g.90712287A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712287A>G , CM000667.2:g.90712287A>G	GRCh38
NC_000005.9:g.90008104A>G , CM000667.1:g.90008104A>G	GRCh37
NC_000005.8:g.90043860A>G	NCBI36
NG_007083.1:g.158488A>G
NG_007083.2:g.187944A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9043A>G MANE Select	ENSP00000384582.2:p.Ile3015Val
ENST00000639431.1:c.265+36078A>G	ENSP00000491057.1:n.265+36078A>G
ENST00000639473.1:n.4502A>G
ENST00000640012.1:c.2850A>G
ENST00000640374.1:n.2187A>G
ENST00000640779.1:c.3772A>G
ENST00000405460.6:c.9043A>G	ENSP00000384582.2:p.Ile3015Val
ENST00000509621.1:c.1740A>G
NM_032119.3:c.9043A>G	NP_115495.3:p.Ile3015Val
NR_003149.1:n.9056A>G
XM_011543675.1:c.9040A>G	XP_011541977.1:p.Ile3014Val
XM_011543676.1:c.8962A>G	XP_011541978.1:p.Ile2988Val
XM_011543677.1:c.6346A>G	XP_011541979.1:p.Ile2116Val
XM_011543678.1:c.9043A>G	XP_011541980.1:p.Ile3015Val
XM_011543679.1:c.9043A>G	XP_011541981.1:p.Ile3015Val
NM_032119.4:c.9043A>G MANE Select	NP_115495.3:p.Ile3015Val
XM_017009963.2:c.9064A>G	XP_016865452.1:p.Ile3022Val
XM_017009964.2:c.9061A>G	XP_016865453.1:p.Ile3021Val
XM_017009965.1:c.9061A>G	XP_016865454.1:p.Ile3021Val
XM_017009966.2:c.8983A>G	XP_016865455.1:p.Ile2995Val
XM_017009967.1:c.8968A>G	XP_016865456.1:p.Ile2990Val
XM_017009968.2:c.9064A>G	XP_016865457.1:p.Ile3022Val
XM_017009969.2:c.9064A>G	XP_016865458.1:p.Ile3022Val
XM_017009970.2:c.9064A>G	XP_016865459.1:p.Ile3022Val
XM_017009971.2:c.9064A>G	XP_016865460.1:p.Ile3022Val
XM_017009972.1:c.2182A>G	XP_016865461.1:p.Ile728Val
XM_017009973.1:c.2161A>G	XP_016865462.1:p.Ile721Val
XM_017009974.2:c.9064A>G	XP_016865463.1:p.Ile3022Val
NR_003149.2:n.9059A>G