Canonical Allele Identifier: CA360397567

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012472A>G (hg19) ; chr5:g.90716655A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9373A>G MANE Select	ENSP00000384582.2:p.Asn3125Asp
ENST00000639431.1:c.265+40446A>G	ENSP00000491057.1:n.265+40446A>G
ENST00000639473.1:n.4832A>G
ENST00000640012.1:c.3180A>G
ENST00000640374.1:n.2517A>G
ENST00000640779.1:c.4102A>G
ENST00000405460.6:c.9373A>G	ENSP00000384582.2:p.Asn3125Asp
ENST00000509621.1:c.2070A>G
NM_032119.3:c.9373A>G	NP_115495.3:p.Asn3125Asp
NR_003149.1:n.9386A>G
XM_011543675.1:c.9370A>G	XP_011541977.1:p.Asn3124Asp
XM_011543676.1:c.9292A>G	XP_011541978.1:p.Asn3098Asp
XM_011543677.1:c.6676A>G	XP_011541979.1:p.Asn2226Asp
XM_011543678.1:c.9373A>G	XP_011541980.1:p.Asn3125Asp
XM_011543679.1:c.9373A>G	XP_011541981.1:p.Asn3125Asp
XR_948560.1:n.272-846T>C
NM_032119.4:c.9373A>G MANE Select	NP_115495.3:p.Asn3125Asp
XM_017009963.2:c.9394A>G	XP_016865452.1:p.Asn3132Asp
XM_017009964.2:c.9391A>G	XP_016865453.1:p.Asn3131Asp
XM_017009965.1:c.9391A>G	XP_016865454.1:p.Asn3131Asp
XM_017009966.2:c.9313A>G	XP_016865455.1:p.Asn3105Asp
XM_017009967.1:c.9298A>G	XP_016865456.1:p.Asn3100Asp
XM_017009968.2:c.9394A>G	XP_016865457.1:p.Asn3132Asp
XM_017009969.2:c.9394A>G	XP_016865458.1:p.Asn3132Asp
XM_017009970.2:c.9394A>G	XP_016865459.1:p.Asn3132Asp
XM_017009971.2:c.9394A>G	XP_016865460.1:p.Asn3132Asp
XM_017009972.1:c.2512A>G	XP_016865461.1:p.Asn838Asp
XM_017009973.1:c.2491A>G	XP_016865462.1:p.Asn831Asp
XM_017009974.2:c.9394A>G	XP_016865463.1:p.Asn3132Asp
XR_001742802.1:n.2523-846T>C
NR_003149.2:n.9389A>G