Canonical Allele Identifier: CA360371707

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90692737-C-T
• MyVariant Identifiers: chr5:g.89988554C>T (hg19) ; chr5:g.90692737C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692737C>T , CM000667.2:g.90692737C>T	GRCh38
NC_000005.9:g.89988554C>T , CM000667.1:g.89988554C>T	GRCh37
NC_000005.8:g.90024310C>T	NCBI36
NG_007083.1:g.138938C>T
NG_007083.2:g.168394C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7084C>T MANE Select	ENSP00000384582.2:p.Gln2362Ter
ENST00000639431.1:c.265+16528C>T	ENSP00000491057.1:n.265+16528C>T
ENST00000639473.1:n.2543C>T
ENST00000640012.1:c.891C>T
ENST00000640374.1:n.228C>T
ENST00000640403.1:c.4375C>T	ENSP00000492531.1:p.Gln1459Ter
ENST00000640779.1:c.1813C>T
ENST00000405460.6:c.7084C>T	ENSP00000384582.2:p.Gln2362Ter
NM_032119.3:c.7084C>T	NP_115495.3:p.Gln2362Ter
NR_003149.1:n.7097C>T
XM_011543675.1:c.7081C>T	XP_011541977.1:p.Gln2361Ter
XM_011543676.1:c.7003C>T	XP_011541978.1:p.Gln2335Ter
XM_011543677.1:c.4387C>T	XP_011541979.1:p.Gln1463Ter
XM_011543678.1:c.7084C>T	XP_011541980.1:p.Gln2362Ter
XM_011543679.1:c.7084C>T	XP_011541981.1:p.Gln2362Ter
NM_032119.4:c.7084C>T MANE Select	NP_115495.3:p.Gln2362Ter
XM_017009963.2:c.7084C>T	XP_016865452.1:p.Gln2362Ter
XM_017009964.2:c.7081C>T	XP_016865453.1:p.Gln2361Ter
XM_017009965.1:c.7081C>T	XP_016865454.1:p.Gln2361Ter
XM_017009966.2:c.7003C>T	XP_016865455.1:p.Gln2335Ter
XM_017009967.1:c.6988C>T	XP_016865456.1:p.Gln2330Ter
XM_017009968.2:c.7084C>T	XP_016865457.1:p.Gln2362Ter
XM_017009969.2:c.7084C>T	XP_016865458.1:p.Gln2362Ter
XM_017009970.2:c.7084C>T	XP_016865459.1:p.Gln2362Ter
XM_017009971.2:c.7084C>T	XP_016865460.1:p.Gln2362Ter
XM_017009972.1:c.202C>T	XP_016865461.1:p.Gln68Ter
XM_017009973.1:c.202C>T	XP_016865462.1:p.Gln68Ter
XM_017009974.2:c.7084C>T	XP_016865463.1:p.Gln2362Ter
NR_003149.2:n.7100C>T