Canonical Allele Identifier: CA360371979

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90692764-G-T
• MyVariant Identifiers: chr5:g.89988581G>T (hg19) ; chr5:g.90692764G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692764G>T , CM000667.2:g.90692764G>T	GRCh38
NC_000005.9:g.89988581G>T , CM000667.1:g.89988581G>T	GRCh37
NC_000005.8:g.90024337G>T	NCBI36
NG_007083.1:g.138965G>T
NG_007083.2:g.168421G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.7111G>T MANE Select	ENSP00000384582.2:p.Ala2371Ser
ENST00000639431.1:c.265+16555G>T	ENSP00000491057.1:n.265+16555G>T
ENST00000639473.1:n.2570G>T
ENST00000640012.1:c.918G>T
ENST00000640374.1:n.255G>T
ENST00000640403.1:c.4402G>T	ENSP00000492531.1:p.Ala1468Ser
ENST00000640779.1:c.1840G>T
ENST00000405460.6:c.7111G>T	ENSP00000384582.2:p.Ala2371Ser
NM_032119.3:c.7111G>T	NP_115495.3:p.Ala2371Ser
NR_003149.1:n.7124G>T
XM_011543675.1:c.7108G>T	XP_011541977.1:p.Ala2370Ser
XM_011543676.1:c.7030G>T	XP_011541978.1:p.Ala2344Ser
XM_011543677.1:c.4414G>T	XP_011541979.1:p.Ala1472Ser
XM_011543678.1:c.7111G>T	XP_011541980.1:p.Ala2371Ser
XM_011543679.1:c.7111G>T	XP_011541981.1:p.Ala2371Ser
NM_032119.4:c.7111G>T MANE Select	NP_115495.3:p.Ala2371Ser
XM_017009963.2:c.7111G>T	XP_016865452.1:p.Ala2371Ser
XM_017009964.2:c.7108G>T	XP_016865453.1:p.Ala2370Ser
XM_017009965.1:c.7108G>T	XP_016865454.1:p.Ala2370Ser
XM_017009966.2:c.7030G>T	XP_016865455.1:p.Ala2344Ser
XM_017009967.1:c.7015G>T	XP_016865456.1:p.Ala2339Ser
XM_017009968.2:c.7111G>T	XP_016865457.1:p.Ala2371Ser
XM_017009969.2:c.7111G>T	XP_016865458.1:p.Ala2371Ser
XM_017009970.2:c.7111G>T	XP_016865459.1:p.Ala2371Ser
XM_017009971.2:c.7111G>T	XP_016865460.1:p.Ala2371Ser
XM_017009972.1:c.229G>T	XP_016865461.1:p.Ala77Ser
XM_017009973.1:c.229G>T	XP_016865462.1:p.Ala77Ser
XM_017009974.2:c.7111G>T	XP_016865463.1:p.Ala2371Ser
NR_003149.2:n.7127G>T