Canonical Allele Identifier: CA360396341

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.90008206A>T (hg19) ; chr5:g.90712389A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90712389A>T , CM000667.2:g.90712389A>T	GRCh38
NC_000005.9:g.90008206A>T , CM000667.1:g.90008206A>T	GRCh37
NC_000005.8:g.90043962A>T	NCBI36
NG_007083.1:g.158590A>T
NG_007083.2:g.188046A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.9145A>T MANE Select	ENSP00000384582.2:p.Asn3049Tyr
ENST00000639431.1:c.265+36180A>T	ENSP00000491057.1:n.265+36180A>T
ENST00000639473.1:n.4604A>T
ENST00000640012.1:c.2952A>T
ENST00000640374.1:n.2289A>T
ENST00000640779.1:c.3874A>T
ENST00000405460.6:c.9145A>T	ENSP00000384582.2:p.Asn3049Tyr
ENST00000509621.1:c.1842A>T
NM_032119.3:c.9145A>T	NP_115495.3:p.Asn3049Tyr
NR_003149.1:n.9158A>T
XM_011543675.1:c.9142A>T	XP_011541977.1:p.Asn3048Tyr
XM_011543676.1:c.9064A>T	XP_011541978.1:p.Asn3022Tyr
XM_011543677.1:c.6448A>T	XP_011541979.1:p.Asn2150Tyr
XM_011543678.1:c.9145A>T	XP_011541980.1:p.Asn3049Tyr
XM_011543679.1:c.9145A>T	XP_011541981.1:p.Asn3049Tyr
XR_948560.1:n.457T>A
NM_032119.4:c.9145A>T MANE Select	NP_115495.3:p.Asn3049Tyr
XM_017009963.2:c.9166A>T	XP_016865452.1:p.Asn3056Tyr
XM_017009964.2:c.9163A>T	XP_016865453.1:p.Asn3055Tyr
XM_017009965.1:c.9163A>T	XP_016865454.1:p.Asn3055Tyr
XM_017009966.2:c.9085A>T	XP_016865455.1:p.Asn3029Tyr
XM_017009967.1:c.9070A>T	XP_016865456.1:p.Asn3024Tyr
XM_017009968.2:c.9166A>T	XP_016865457.1:p.Asn3056Tyr
XM_017009969.2:c.9166A>T	XP_016865458.1:p.Asn3056Tyr
XM_017009970.2:c.9166A>T	XP_016865459.1:p.Asn3056Tyr
XM_017009971.2:c.9166A>T	XP_016865460.1:p.Asn3056Tyr
XM_017009972.1:c.2284A>T	XP_016865461.1:p.Asn762Tyr
XM_017009973.1:c.2263A>T	XP_016865462.1:p.Asn755Tyr
XM_017009974.2:c.9166A>T	XP_016865463.1:p.Asn3056Tyr
NR_003149.2:n.9161A>T