Canonical Allele Identifier: CA2674568628

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90744908-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90744908T>C , CM000667.2:g.90744908T>C	GRCh38
NC_000005.9:g.90040725T>C , CM000667.1:g.90040725T>C	GRCh37
NC_000005.8:g.90076481T>C	NCBI36
NG_007083.1:g.191109T>C
NG_007083.2:g.220565T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.10550-138T>C MANE Select	ENSP00000384582.2:n.10550-138T>C
ENST00000639431.1:c.265+68699T>C	ENSP00000491057.1:n.265+68699T>C
ENST00000640374.1:n.3694-138T>C
ENST00000640464.1:n.969-138T>C
ENST00000405460.6:c.10550-138T>C	ENSP00000384582.2:n.10550-138T>C
ENST00000509621.1:c.3247-138T>C
NM_032119.3:c.10550-138T>C	NP_115495.3:n.10550-138T>C
NR_003149.1:n.10563-138T>C
XM_011543675.1:c.10547-138T>C	XP_011541977.1:n.10547-138T>C
XM_011543676.1:c.10469-138T>C	XP_011541978.1:n.10469-138T>C
XM_011543677.1:c.7853-138T>C	XP_011541979.1:n.7853-138T>C
XM_011543678.1:c.10550-138T>C	XP_011541980.1:n.10550-138T>C
XM_011543679.1:c.10550-138T>C	XP_011541981.1:n.10550-138T>C
NM_032119.4:c.10550-138T>C MANE Select	NP_115495.3:n.10550-138T>C
XM_017009963.2:c.10571-138T>C	XP_016865452.1:n.10571-138T>C
XM_017009964.2:c.10568-138T>C	XP_016865453.1:n.10568-138T>C
XM_017009965.1:c.10568-138T>C	XP_016865454.1:n.10568-138T>C
XM_017009966.2:c.10490-138T>C	XP_016865455.1:n.10490-138T>C
XM_017009967.1:c.10475-138T>C	XP_016865456.1:n.10475-138T>C
XM_017009968.2:c.10571-138T>C	XP_016865457.1:n.10571-138T>C
XM_017009969.2:c.10571-138T>C	XP_016865458.1:n.10571-138T>C
XM_017009970.2:c.10571-138T>C	XP_016865459.1:n.10571-138T>C
XM_017009971.2:c.10571-138T>C	XP_016865460.1:n.10571-138T>C
XM_017009972.1:c.3689-138T>C	XP_016865461.1:n.3689-138T>C
XM_017009973.1:c.3668-138T>C	XP_016865462.1:n.3668-138T>C
XM_017009974.2:c.10571-138T>C	XP_016865463.1:n.10571-138T>C
NR_003149.2:n.10566-138T>C