Canonical Allele Identifier: CA122808865

Gene: ADGRV1

Linked Data

• dbSNP Id: rs532764958
• gnomAD v2: 5-90020477-G-T
• gnomAD v3: 5-90724660-G-T
• gnomAD v4: 5-90724660-G-T
• MyVariant Identifiers: chr5:g.90020477G>T (hg19) ; chr5:g.90724660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90724660G>T , CM000667.2:g.90724660G>T	GRCh38
NC_000005.9:g.90020477G>T , CM000667.1:g.90020477G>T	GRCh37
NC_000005.8:g.90056233G>T	NCBI36
NG_007083.1:g.170861G>T
NG_007083.2:g.200317G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9749-172G>T MANE Select	ENSP00000384582.2:n.9749-172G>T
ENST00000639431.1:c.265+48451G>T	ENSP00000491057.1:n.265+48451G>T
ENST00000640374.1:n.2893-172G>T
ENST00000640464.1:n.168-172G>T
ENST00000640779.1:c.4478-172G>T
ENST00000405460.6:c.9749-172G>T	ENSP00000384582.2:n.9749-172G>T
ENST00000509621.1:c.2446-172G>T
NM_032119.3:c.9749-172G>T	NP_115495.3:n.9749-172G>T
NR_003149.1:n.9762-172G>T
XM_011543675.1:c.9746-172G>T	XP_011541977.1:n.9746-172G>T
XM_011543676.1:c.9668-172G>T	XP_011541978.1:n.9668-172G>T
XM_011543677.1:c.7052-172G>T	XP_011541979.1:n.7052-172G>T
XM_011543678.1:c.9749-172G>T	XP_011541980.1:n.9749-172G>T
XM_011543679.1:c.9749-172G>T	XP_011541981.1:n.9749-172G>T
XR_948560.1:n.272-8851C>A
NM_032119.4:c.9749-172G>T MANE Select	NP_115495.3:n.9749-172G>T
XM_017009963.2:c.9770-172G>T	XP_016865452.1:n.9770-172G>T
XM_017009964.2:c.9767-172G>T	XP_016865453.1:n.9767-172G>T
XM_017009965.1:c.9767-172G>T	XP_016865454.1:n.9767-172G>T
XM_017009966.2:c.9689-172G>T	XP_016865455.1:n.9689-172G>T
XM_017009967.1:c.9674-172G>T	XP_016865456.1:n.9674-172G>T
XM_017009968.2:c.9770-172G>T	XP_016865457.1:n.9770-172G>T
XM_017009969.2:c.9770-172G>T	XP_016865458.1:n.9770-172G>T
XM_017009970.2:c.9770-172G>T	XP_016865459.1:n.9770-172G>T
XM_017009971.2:c.9770-172G>T	XP_016865460.1:n.9770-172G>T
XM_017009972.1:c.2888-172G>T	XP_016865461.1:n.2888-172G>T
XM_017009973.1:c.2867-172G>T	XP_016865462.1:n.2867-172G>T
XM_017009974.2:c.9770-172G>T	XP_016865463.1:n.9770-172G>T
XR_001742802.1:n.2523-8851C>A
NR_003149.2:n.9765-172G>T