Canonical Allele Identifier: CA360414221

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90684066-T-G
• MyVariant Identifiers: chr5:g.89979883T>G (hg19) ; chr5:g.90684066T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684066T>G , CM000667.2:g.90684066T>G	GRCh38
NC_000005.9:g.89979883T>G , CM000667.1:g.89979883T>G	GRCh37
NC_000005.8:g.90015639T>G	NCBI36
NG_007083.1:g.130267T>G
NG_007083.2:g.159723T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6145T>G MANE Select	ENSP00000384582.2:p.Phe2049Val
ENST00000639431.1:c.265+7857T>G	ENSP00000491057.1:n.265+7857T>G
ENST00000639473.1:n.1604T>G
ENST00000640012.1:c.165-1714T>G
ENST00000640403.1:c.3436T>G	ENSP00000492531.1:p.Phe1146Val
ENST00000640779.1:c.957T>G
ENST00000405460.6:c.6145T>G	ENSP00000384582.2:p.Phe2049Val
NM_032119.3:c.6145T>G	NP_115495.3:p.Phe2049Val
NR_003149.1:n.6241T>G
XM_011543675.1:c.6142T>G	XP_011541977.1:p.Phe2048Val
XM_011543676.1:c.6064T>G	XP_011541978.1:p.Phe2022Val
XM_011543677.1:c.3448T>G	XP_011541979.1:p.Phe1150Val
XM_011543678.1:c.6145T>G	XP_011541980.1:p.Phe2049Val
XM_011543679.1:c.6145T>G	XP_011541981.1:p.Phe2049Val
NM_032119.4:c.6145T>G MANE Select	NP_115495.3:p.Phe2049Val
XM_017009963.2:c.6145T>G	XP_016865452.1:p.Phe2049Val
XM_017009964.2:c.6142T>G	XP_016865453.1:p.Phe2048Val
XM_017009965.1:c.6142T>G	XP_016865454.1:p.Phe2048Val
XM_017009966.2:c.6064T>G	XP_016865455.1:p.Phe2022Val
XM_017009967.1:c.6049T>G	XP_016865456.1:p.Phe2017Val
XM_017009968.2:c.6145T>G	XP_016865457.1:p.Phe2049Val
XM_017009969.2:c.6145T>G	XP_016865458.1:p.Phe2049Val
XM_017009970.2:c.6145T>G	XP_016865459.1:p.Phe2049Val
XM_017009971.2:c.6145T>G	XP_016865460.1:p.Phe2049Val
XM_017009973.1:c.-655T>G	XP_016865462.1:n.-655T>G
XM_017009974.2:c.6145T>G	XP_016865463.1:p.Phe2049Val
NR_003149.2:n.6244T>G