Canonical Allele Identifier: CA360397606

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90012482A>T (hg19) ; chr5:g.90716665A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90716665A>T , CM000667.2:g.90716665A>T	GRCh38
NC_000005.9:g.90012482A>T , CM000667.1:g.90012482A>T	GRCh37
NC_000005.8:g.90048238A>T	NCBI36
NG_007083.1:g.162866A>T
NG_007083.2:g.192322A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9383A>T MANE Select	ENSP00000384582.2:p.Asn3128Ile
ENST00000639431.1:c.265+40456A>T	ENSP00000491057.1:n.265+40456A>T
ENST00000639473.1:n.4842A>T
ENST00000640012.1:c.3190A>T
ENST00000640374.1:n.2527A>T
ENST00000640779.1:c.4112A>T
ENST00000405460.6:c.9383A>T	ENSP00000384582.2:p.Asn3128Ile
ENST00000509621.1:c.2080A>T
NM_032119.3:c.9383A>T	NP_115495.3:p.Asn3128Ile
NR_003149.1:n.9396A>T
XM_011543675.1:c.9380A>T	XP_011541977.1:p.Asn3127Ile
XM_011543676.1:c.9302A>T	XP_011541978.1:p.Asn3101Ile
XM_011543677.1:c.6686A>T	XP_011541979.1:p.Asn2229Ile
XM_011543678.1:c.9383A>T	XP_011541980.1:p.Asn3128Ile
XM_011543679.1:c.9383A>T	XP_011541981.1:p.Asn3128Ile
XR_948560.1:n.272-856T>A
NM_032119.4:c.9383A>T MANE Select	NP_115495.3:p.Asn3128Ile
XM_017009963.2:c.9404A>T	XP_016865452.1:p.Asn3135Ile
XM_017009964.2:c.9401A>T	XP_016865453.1:p.Asn3134Ile
XM_017009965.1:c.9401A>T	XP_016865454.1:p.Asn3134Ile
XM_017009966.2:c.9323A>T	XP_016865455.1:p.Asn3108Ile
XM_017009967.1:c.9308A>T	XP_016865456.1:p.Asn3103Ile
XM_017009968.2:c.9404A>T	XP_016865457.1:p.Asn3135Ile
XM_017009969.2:c.9404A>T	XP_016865458.1:p.Asn3135Ile
XM_017009970.2:c.9404A>T	XP_016865459.1:p.Asn3135Ile
XM_017009971.2:c.9404A>T	XP_016865460.1:p.Asn3135Ile
XM_017009972.1:c.2522A>T	XP_016865461.1:p.Asn841Ile
XM_017009973.1:c.2501A>T	XP_016865462.1:p.Asn834Ile
XM_017009974.2:c.9404A>T	XP_016865463.1:p.Asn3135Ile
XR_001742802.1:n.2523-856T>A
NR_003149.2:n.9399A>T