Canonical Allele Identifier: CA360397568

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90716655-A-T
• MyVariant Identifiers: chr5:g.90012472A>T (hg19) ; chr5:g.90716655A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716655A>T , CM000667.2:g.90716655A>T	GRCh38
NC_000005.9:g.90012472A>T , CM000667.1:g.90012472A>T	GRCh37
NC_000005.8:g.90048228A>T	NCBI36
NG_007083.1:g.162856A>T
NG_007083.2:g.192312A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9373A>T MANE Select	ENSP00000384582.2:p.Asn3125Tyr
ENST00000639431.1:c.265+40446A>T	ENSP00000491057.1:n.265+40446A>T
ENST00000639473.1:n.4832A>T
ENST00000640012.1:c.3180A>T
ENST00000640374.1:n.2517A>T
ENST00000640779.1:c.4102A>T
ENST00000405460.6:c.9373A>T	ENSP00000384582.2:p.Asn3125Tyr
ENST00000509621.1:c.2070A>T
NM_032119.3:c.9373A>T	NP_115495.3:p.Asn3125Tyr
NR_003149.1:n.9386A>T
XM_011543675.1:c.9370A>T	XP_011541977.1:p.Asn3124Tyr
XM_011543676.1:c.9292A>T	XP_011541978.1:p.Asn3098Tyr
XM_011543677.1:c.6676A>T	XP_011541979.1:p.Asn2226Tyr
XM_011543678.1:c.9373A>T	XP_011541980.1:p.Asn3125Tyr
XM_011543679.1:c.9373A>T	XP_011541981.1:p.Asn3125Tyr
XR_948560.1:n.272-846T>A
NM_032119.4:c.9373A>T MANE Select	NP_115495.3:p.Asn3125Tyr
XM_017009963.2:c.9394A>T	XP_016865452.1:p.Asn3132Tyr
XM_017009964.2:c.9391A>T	XP_016865453.1:p.Asn3131Tyr
XM_017009965.1:c.9391A>T	XP_016865454.1:p.Asn3131Tyr
XM_017009966.2:c.9313A>T	XP_016865455.1:p.Asn3105Tyr
XM_017009967.1:c.9298A>T	XP_016865456.1:p.Asn3100Tyr
XM_017009968.2:c.9394A>T	XP_016865457.1:p.Asn3132Tyr
XM_017009969.2:c.9394A>T	XP_016865458.1:p.Asn3132Tyr
XM_017009970.2:c.9394A>T	XP_016865459.1:p.Asn3132Tyr
XM_017009971.2:c.9394A>T	XP_016865460.1:p.Asn3132Tyr
XM_017009972.1:c.2512A>T	XP_016865461.1:p.Asn838Tyr
XM_017009973.1:c.2491A>T	XP_016865462.1:p.Asn831Tyr
XM_017009974.2:c.9394A>T	XP_016865463.1:p.Asn3132Tyr
XR_001742802.1:n.2523-846T>A
NR_003149.2:n.9389A>T