Canonical Allele Identifier: CA360414240

Gene: ADGRV1

Linked Data

• MyVariant Identifiers: chr5:g.89979892A>G (hg19) ; chr5:g.90684075A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90684075A>G , CM000667.2:g.90684075A>G	GRCh38
NC_000005.9:g.89979892A>G , CM000667.1:g.89979892A>G	GRCh37
NC_000005.8:g.90015648A>G	NCBI36
NG_007083.1:g.130276A>G
NG_007083.2:g.159732A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6154A>G MANE Select	ENSP00000384582.2:p.Asn2052Asp
ENST00000639431.1:c.265+7866A>G	ENSP00000491057.1:n.265+7866A>G
ENST00000639473.1:n.1613A>G
ENST00000640012.1:c.165-1705A>G
ENST00000640403.1:c.3445A>G	ENSP00000492531.1:p.Asn1149Asp
ENST00000640779.1:c.966A>G
ENST00000405460.6:c.6154A>G	ENSP00000384582.2:p.Asn2052Asp
NM_032119.3:c.6154A>G	NP_115495.3:p.Asn2052Asp
NR_003149.1:n.6250A>G
XM_011543675.1:c.6151A>G	XP_011541977.1:p.Asn2051Asp
XM_011543676.1:c.6073A>G	XP_011541978.1:p.Asn2025Asp
XM_011543677.1:c.3457A>G	XP_011541979.1:p.Asn1153Asp
XM_011543678.1:c.6154A>G	XP_011541980.1:p.Asn2052Asp
XM_011543679.1:c.6154A>G	XP_011541981.1:p.Asn2052Asp
NM_032119.4:c.6154A>G MANE Select	NP_115495.3:p.Asn2052Asp
XM_017009963.2:c.6154A>G	XP_016865452.1:p.Asn2052Asp
XM_017009964.2:c.6151A>G	XP_016865453.1:p.Asn2051Asp
XM_017009965.1:c.6151A>G	XP_016865454.1:p.Asn2051Asp
XM_017009966.2:c.6073A>G	XP_016865455.1:p.Asn2025Asp
XM_017009967.1:c.6058A>G	XP_016865456.1:p.Asn2020Asp
XM_017009968.2:c.6154A>G	XP_016865457.1:p.Asn2052Asp
XM_017009969.2:c.6154A>G	XP_016865458.1:p.Asn2052Asp
XM_017009970.2:c.6154A>G	XP_016865459.1:p.Asn2052Asp
XM_017009971.2:c.6154A>G	XP_016865460.1:p.Asn2052Asp
XM_017009973.1:c.-646A>G	XP_016865462.1:n.-646A>G
XM_017009974.2:c.6154A>G	XP_016865463.1:p.Asn2052Asp
NR_003149.2:n.6253A>G