Canonical Allele Identifier: CA360371358

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90692696-C-A
• MyVariant Identifiers: chr5:g.89988513C>A (hg19) ; chr5:g.90692696C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692696C>A , CM000667.2:g.90692696C>A	GRCh38
NC_000005.9:g.89988513C>A , CM000667.1:g.89988513C>A	GRCh37
NC_000005.8:g.90024269C>A	NCBI36
NG_007083.1:g.138897C>A
NG_007083.2:g.168353C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7043C>A MANE Select	ENSP00000384582.2:p.Pro2348His
ENST00000639431.1:c.265+16487C>A	ENSP00000491057.1:n.265+16487C>A
ENST00000639473.1:n.2502C>A
ENST00000640012.1:c.850C>A
ENST00000640374.1:n.187C>A
ENST00000640403.1:c.4334C>A	ENSP00000492531.1:p.Pro1445His
ENST00000640779.1:c.1772C>A
ENST00000405460.6:c.7043C>A	ENSP00000384582.2:p.Pro2348His
NM_032119.3:c.7043C>A	NP_115495.3:p.Pro2348His
NR_003149.1:n.7056C>A
XM_011543675.1:c.7040C>A	XP_011541977.1:p.Pro2347His
XM_011543676.1:c.6962C>A	XP_011541978.1:p.Pro2321His
XM_011543677.1:c.4346C>A	XP_011541979.1:p.Pro1449His
XM_011543678.1:c.7043C>A	XP_011541980.1:p.Pro2348His
XM_011543679.1:c.7043C>A	XP_011541981.1:p.Pro2348His
NM_032119.4:c.7043C>A MANE Select	NP_115495.3:p.Pro2348His
XM_017009963.2:c.7043C>A	XP_016865452.1:p.Pro2348His
XM_017009964.2:c.7040C>A	XP_016865453.1:p.Pro2347His
XM_017009965.1:c.7040C>A	XP_016865454.1:p.Pro2347His
XM_017009966.2:c.6962C>A	XP_016865455.1:p.Pro2321His
XM_017009967.1:c.6947C>A	XP_016865456.1:p.Pro2316His
XM_017009968.2:c.7043C>A	XP_016865457.1:p.Pro2348His
XM_017009969.2:c.7043C>A	XP_016865458.1:p.Pro2348His
XM_017009970.2:c.7043C>A	XP_016865459.1:p.Pro2348His
XM_017009971.2:c.7043C>A	XP_016865460.1:p.Pro2348His
XM_017009972.1:c.161C>A	XP_016865461.1:p.Pro54His
XM_017009973.1:c.161C>A	XP_016865462.1:p.Pro54His
XM_017009974.2:c.7043C>A	XP_016865463.1:p.Pro2348His
NR_003149.2:n.7059C>A