Canonical Allele Identifier: CA560901504

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1374581613
• gnomAD v2: 5-90020480-GTTATT-G
• gnomAD v3: 5-90724663-GTTATT-G
• gnomAD v4: 5-90724663-GTTATT-G
• MyVariant Identifiers: chr5:g.90020481_90020485del (hg19) ; chr5:g.90724664_90724668del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90724667_90724671del , CM000667.2:g.90724667_90724671del	GRCh38
NC_000005.9:g.90020484_90020488del , CM000667.1:g.90020484_90020488del	GRCh37
NC_000005.8:g.90056240_90056244del	NCBI36
NG_007083.1:g.170868_170872del
NG_007083.2:g.200324_200328del

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9749-165_9749-161del MANE Select	ENSP00000384582.2:n.9749-165_9749-161del
ENST00000639431.1:c.265+48458_265+48462del	ENSP00000491057.1:n.265+48458_265+48462del
ENST00000640374.1:n.2893-165_2893-161del
ENST00000640464.1:n.168-165_168-161del
ENST00000640779.1:c.4478-165_4478-161del
ENST00000405460.6:c.9749-165_9749-161del	ENSP00000384582.2:n.9749-165_9749-161del
ENST00000509621.1:c.2446-165_2446-161del
NM_032119.3:c.9749-165_9749-161del	NP_115495.3:n.9749-165_9749-161del
NR_003149.1:n.9762-165_9762-161del
XM_011543675.1:c.9746-165_9746-161del	XP_011541977.1:n.9746-165_9746-161del
XM_011543676.1:c.9668-165_9668-161del	XP_011541978.1:n.9668-165_9668-161del
XM_011543677.1:c.7052-165_7052-161del	XP_011541979.1:n.7052-165_7052-161del
XM_011543678.1:c.9749-165_9749-161del	XP_011541980.1:n.9749-165_9749-161del
XM_011543679.1:c.9749-165_9749-161del	XP_011541981.1:n.9749-165_9749-161del
XR_948560.1:n.272-8859_272-8855del
NM_032119.4:c.9749-165_9749-161del MANE Select	NP_115495.3:n.9749-165_9749-161del
XM_017009963.2:c.9770-165_9770-161del	XP_016865452.1:n.9770-165_9770-161del
XM_017009964.2:c.9767-165_9767-161del	XP_016865453.1:n.9767-165_9767-161del
XM_017009965.1:c.9767-165_9767-161del	XP_016865454.1:n.9767-165_9767-161del
XM_017009966.2:c.9689-165_9689-161del	XP_016865455.1:n.9689-165_9689-161del
XM_017009967.1:c.9674-165_9674-161del	XP_016865456.1:n.9674-165_9674-161del
XM_017009968.2:c.9770-165_9770-161del	XP_016865457.1:n.9770-165_9770-161del
XM_017009969.2:c.9770-165_9770-161del	XP_016865458.1:n.9770-165_9770-161del
XM_017009970.2:c.9770-165_9770-161del	XP_016865459.1:n.9770-165_9770-161del
XM_017009971.2:c.9770-165_9770-161del	XP_016865460.1:n.9770-165_9770-161del
XM_017009972.1:c.2888-165_2888-161del	XP_016865461.1:n.2888-165_2888-161del
XM_017009973.1:c.2867-165_2867-161del	XP_016865462.1:n.2867-165_2867-161del
XM_017009974.2:c.9770-165_9770-161del	XP_016865463.1:n.9770-165_9770-161del
XR_001742802.1:n.2523-8859_2523-8855del
NR_003149.2:n.9765-165_9765-161del