Canonical Allele Identifier: CA121835155

Gene: ADGRV1

Linked Data

• ClinVar Variation Id: 2778220
• ClinVar RCV Id: RCV003661339
• dbSNP Id: rs940362895
• gnomAD v2: 5-89940698-A-G
• gnomAD v3: 5-90644881-A-G
• gnomAD v4: 5-90644881-A-G
• MyVariant Identifiers: chr5:g.89940698A>G (hg19) ; chr5:g.90644881A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90644881A>G , CM000667.2:g.90644881A>G	GRCh38
NC_000005.9:g.89940698A>G , CM000667.1:g.89940698A>G	GRCh37
NC_000005.8:g.89976454A>G	NCBI36
NG_007083.1:g.91082A>G
NG_007083.2:g.120538A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.2898+12A>G MANE Select	ENSP00000384582.2:n.2898+12A>G
ENST00000504142.2:n.1664+12A>G
ENST00000639676.1:n.496+12A>G
ENST00000640403.1:c.201+12A>G	ENSP00000492531.1:n.201+12A>G
ENST00000405460.6:c.2898+12A>G	ENSP00000384582.2:n.2898+12A>G
ENST00000504142.1:c.1663+12A>G
NM_032119.3:c.2898+12A>G	NP_115495.3:n.2898+12A>G
NR_003149.1:n.2994+12A>G
XM_011543675.1:c.2898+12A>G	XP_011541977.1:n.2898+12A>G
XM_011543676.1:c.2898+12A>G	XP_011541978.1:n.2898+12A>G
XM_011543677.1:c.201+12A>G	XP_011541979.1:n.201+12A>G
XM_011543678.1:c.2898+12A>G	XP_011541980.1:n.2898+12A>G
XM_011543679.1:c.2898+12A>G	XP_011541981.1:n.2898+12A>G
NM_032119.4:c.2898+12A>G MANE Select	NP_115495.3:n.2898+12A>G
XM_017009963.2:c.2898+12A>G	XP_016865452.1:n.2898+12A>G
XM_017009964.2:c.2898+12A>G	XP_016865453.1:n.2898+12A>G
XM_017009965.1:c.2895+12A>G	XP_016865454.1:n.2895+12A>G
XM_017009966.2:c.2898+12A>G	XP_016865455.1:n.2898+12A>G
XM_017009967.1:c.2802+12A>G	XP_016865456.1:n.2802+12A>G
XM_017009968.2:c.2898+12A>G	XP_016865457.1:n.2898+12A>G
XM_017009969.2:c.2898+12A>G	XP_016865458.1:n.2898+12A>G
XM_017009970.2:c.2898+12A>G	XP_016865459.1:n.2898+12A>G
XM_017009971.2:c.2898+12A>G	XP_016865460.1:n.2898+12A>G
XM_017009974.2:c.2898+12A>G	XP_016865463.1:n.2898+12A>G
NR_003149.2:n.2997+12A>G