Canonical Allele Identifier: CA360397572

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90716656-A-T
• MyVariant Identifiers: chr5:g.90012473A>T (hg19) ; chr5:g.90716656A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716656A>T , CM000667.2:g.90716656A>T	GRCh38
NC_000005.9:g.90012473A>T , CM000667.1:g.90012473A>T	GRCh37
NC_000005.8:g.90048229A>T	NCBI36
NG_007083.1:g.162857A>T
NG_007083.2:g.192313A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.9374A>T MANE Select	ENSP00000384582.2:p.Asn3125Ile
ENST00000639431.1:c.265+40447A>T	ENSP00000491057.1:n.265+40447A>T
ENST00000639473.1:n.4833A>T
ENST00000640012.1:c.3181A>T
ENST00000640374.1:n.2518A>T
ENST00000640779.1:c.4103A>T
ENST00000405460.6:c.9374A>T	ENSP00000384582.2:p.Asn3125Ile
ENST00000509621.1:c.2071A>T
NM_032119.3:c.9374A>T	NP_115495.3:p.Asn3125Ile
NR_003149.1:n.9387A>T
XM_011543675.1:c.9371A>T	XP_011541977.1:p.Asn3124Ile
XM_011543676.1:c.9293A>T	XP_011541978.1:p.Asn3098Ile
XM_011543677.1:c.6677A>T	XP_011541979.1:p.Asn2226Ile
XM_011543678.1:c.9374A>T	XP_011541980.1:p.Asn3125Ile
XM_011543679.1:c.9374A>T	XP_011541981.1:p.Asn3125Ile
XR_948560.1:n.272-847T>A
NM_032119.4:c.9374A>T MANE Select	NP_115495.3:p.Asn3125Ile
XM_017009963.2:c.9395A>T	XP_016865452.1:p.Asn3132Ile
XM_017009964.2:c.9392A>T	XP_016865453.1:p.Asn3131Ile
XM_017009965.1:c.9392A>T	XP_016865454.1:p.Asn3131Ile
XM_017009966.2:c.9314A>T	XP_016865455.1:p.Asn3105Ile
XM_017009967.1:c.9299A>T	XP_016865456.1:p.Asn3100Ile
XM_017009968.2:c.9395A>T	XP_016865457.1:p.Asn3132Ile
XM_017009969.2:c.9395A>T	XP_016865458.1:p.Asn3132Ile
XM_017009970.2:c.9395A>T	XP_016865459.1:p.Asn3132Ile
XM_017009971.2:c.9395A>T	XP_016865460.1:p.Asn3132Ile
XM_017009972.1:c.2513A>T	XP_016865461.1:p.Asn838Ile
XM_017009973.1:c.2492A>T	XP_016865462.1:p.Asn831Ile
XM_017009974.2:c.9395A>T	XP_016865463.1:p.Asn3132Ile
XR_001742802.1:n.2523-847T>A
NR_003149.2:n.9390A>T