Canonical Allele Identifier: CA360397599

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012481A>G (hg19) ; chr5:g.90716664A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716664A>G , CM000667.2:g.90716664A>G	GRCh38
NC_000005.9:g.90012481A>G , CM000667.1:g.90012481A>G	GRCh37
NC_000005.8:g.90048237A>G	NCBI36
NG_007083.1:g.162865A>G
NG_007083.2:g.192321A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9382A>G MANE Select	ENSP00000384582.2:p.Asn3128Asp
ENST00000639431.1:c.265+40455A>G	ENSP00000491057.1:n.265+40455A>G
ENST00000639473.1:n.4841A>G
ENST00000640012.1:c.3189A>G
ENST00000640374.1:n.2526A>G
ENST00000640779.1:c.4111A>G
ENST00000405460.6:c.9382A>G	ENSP00000384582.2:p.Asn3128Asp
ENST00000509621.1:c.2079A>G
NM_032119.3:c.9382A>G	NP_115495.3:p.Asn3128Asp
NR_003149.1:n.9395A>G
XM_011543675.1:c.9379A>G	XP_011541977.1:p.Asn3127Asp
XM_011543676.1:c.9301A>G	XP_011541978.1:p.Asn3101Asp
XM_011543677.1:c.6685A>G	XP_011541979.1:p.Asn2229Asp
XM_011543678.1:c.9382A>G	XP_011541980.1:p.Asn3128Asp
XM_011543679.1:c.9382A>G	XP_011541981.1:p.Asn3128Asp
XR_948560.1:n.272-855T>C
NM_032119.4:c.9382A>G MANE Select	NP_115495.3:p.Asn3128Asp
XM_017009963.2:c.9403A>G	XP_016865452.1:p.Asn3135Asp
XM_017009964.2:c.9400A>G	XP_016865453.1:p.Asn3134Asp
XM_017009965.1:c.9400A>G	XP_016865454.1:p.Asn3134Asp
XM_017009966.2:c.9322A>G	XP_016865455.1:p.Asn3108Asp
XM_017009967.1:c.9307A>G	XP_016865456.1:p.Asn3103Asp
XM_017009968.2:c.9403A>G	XP_016865457.1:p.Asn3135Asp
XM_017009969.2:c.9403A>G	XP_016865458.1:p.Asn3135Asp
XM_017009970.2:c.9403A>G	XP_016865459.1:p.Asn3135Asp
XM_017009971.2:c.9403A>G	XP_016865460.1:p.Asn3135Asp
XM_017009972.1:c.2521A>G	XP_016865461.1:p.Asn841Asp
XM_017009973.1:c.2500A>G	XP_016865462.1:p.Asn834Asp
XM_017009974.2:c.9403A>G	XP_016865463.1:p.Asn3135Asp
XR_001742802.1:n.2523-855T>C
NR_003149.2:n.9398A>G