Canonical Allele Identifier: CA360414241

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1466249181
• gnomAD v3: 5-90684075-A-T
• gnomAD v4: 5-90684075-A-T
• MyVariant Identifiers: chr5:g.89979892A>T (hg19) ; chr5:g.90684075A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.6154A>T MANE Select	ENSP00000384582.2:p.Asn2052Tyr
ENST00000639431.1:c.265+7866A>T	ENSP00000491057.1:n.265+7866A>T
ENST00000639473.1:n.1613A>T
ENST00000640012.1:c.165-1705A>T
ENST00000640403.1:c.3445A>T	ENSP00000492531.1:p.Asn1149Tyr
ENST00000640779.1:c.966A>T
ENST00000405460.6:c.6154A>T	ENSP00000384582.2:p.Asn2052Tyr
NM_032119.3:c.6154A>T	NP_115495.3:p.Asn2052Tyr
NR_003149.1:n.6250A>T
XM_011543675.1:c.6151A>T	XP_011541977.1:p.Asn2051Tyr
XM_011543676.1:c.6073A>T	XP_011541978.1:p.Asn2025Tyr
XM_011543677.1:c.3457A>T	XP_011541979.1:p.Asn1153Tyr
XM_011543678.1:c.6154A>T	XP_011541980.1:p.Asn2052Tyr
XM_011543679.1:c.6154A>T	XP_011541981.1:p.Asn2052Tyr
NM_032119.4:c.6154A>T MANE Select	NP_115495.3:p.Asn2052Tyr
XM_017009963.2:c.6154A>T	XP_016865452.1:p.Asn2052Tyr
XM_017009964.2:c.6151A>T	XP_016865453.1:p.Asn2051Tyr
XM_017009965.1:c.6151A>T	XP_016865454.1:p.Asn2051Tyr
XM_017009966.2:c.6073A>T	XP_016865455.1:p.Asn2025Tyr
XM_017009967.1:c.6058A>T	XP_016865456.1:p.Asn2020Tyr
XM_017009968.2:c.6154A>T	XP_016865457.1:p.Asn2052Tyr
XM_017009969.2:c.6154A>T	XP_016865458.1:p.Asn2052Tyr
XM_017009970.2:c.6154A>T	XP_016865459.1:p.Asn2052Tyr
XM_017009971.2:c.6154A>T	XP_016865460.1:p.Asn2052Tyr
XM_017009973.1:c.-646A>T	XP_016865462.1:n.-646A>T
XM_017009974.2:c.6154A>T	XP_016865463.1:p.Asn2052Tyr
NR_003149.2:n.6253A>T