Canonical Allele Identifier: CA360414500

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90684193-C-A
• MyVariant Identifiers: chr5:g.89980010C>A (hg19) ; chr5:g.90684193C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684193C>A , CM000667.2:g.90684193C>A	GRCh38
NC_000005.9:g.89980010C>A , CM000667.1:g.89980010C>A	GRCh37
NC_000005.8:g.90015766C>A	NCBI36
NG_007083.1:g.130394C>A
NG_007083.2:g.159850C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.6272C>A MANE Select	ENSP00000384582.2:p.Ser2091Ter
ENST00000639431.1:c.265+7984C>A	ENSP00000491057.1:n.265+7984C>A
ENST00000639473.1:n.1731C>A
ENST00000640012.1:c.165-1587C>A
ENST00000640403.1:c.3563C>A	ENSP00000492531.1:p.Ser1188Ter
ENST00000640779.1:c.1084C>A
ENST00000405460.6:c.6272C>A	ENSP00000384582.2:p.Ser2091Ter
NM_032119.3:c.6272C>A	NP_115495.3:p.Ser2091Ter
NR_003149.1:n.6368C>A
XM_011543675.1:c.6269C>A	XP_011541977.1:p.Ser2090Ter
XM_011543676.1:c.6191C>A	XP_011541978.1:p.Ser2064Ter
XM_011543677.1:c.3575C>A	XP_011541979.1:p.Ser1192Ter
XM_011543678.1:c.6272C>A	XP_011541980.1:p.Ser2091Ter
XM_011543679.1:c.6272C>A	XP_011541981.1:p.Ser2091Ter
NM_032119.4:c.6272C>A MANE Select	NP_115495.3:p.Ser2091Ter
XM_017009963.2:c.6272C>A	XP_016865452.1:p.Ser2091Ter
XM_017009964.2:c.6269C>A	XP_016865453.1:p.Ser2090Ter
XM_017009965.1:c.6269C>A	XP_016865454.1:p.Ser2090Ter
XM_017009966.2:c.6191C>A	XP_016865455.1:p.Ser2064Ter
XM_017009967.1:c.6176C>A	XP_016865456.1:p.Ser2059Ter
XM_017009968.2:c.6272C>A	XP_016865457.1:p.Ser2091Ter
XM_017009969.2:c.6272C>A	XP_016865458.1:p.Ser2091Ter
XM_017009970.2:c.6272C>A	XP_016865459.1:p.Ser2091Ter
XM_017009971.2:c.6272C>A	XP_016865460.1:p.Ser2091Ter
XM_017009973.1:c.-528C>A	XP_016865462.1:n.-528C>A
XM_017009974.2:c.6272C>A	XP_016865463.1:p.Ser2091Ter
NR_003149.2:n.6371C>A