Canonical Allele Identifier: CA445404493

Gene: ADGRV1

Linked Data

• ClinVar Variation Id: 1647413
• ClinVar RCV Id: RCV002139093
• dbSNP Id: rs753961140
• gnomAD v2: 5-89988475-T-C
• gnomAD v4: 5-90692658-T-C
• MyVariant Identifiers: chr5:g.89988475T>C (hg19) ; chr5:g.90692658T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90692658T>C , CM000667.2:g.90692658T>C	GRCh38
NC_000005.9:g.89988475T>C , CM000667.1:g.89988475T>C	GRCh37
NC_000005.8:g.90024231T>C	NCBI36
NG_007083.1:g.138859T>C
NG_007083.2:g.168315T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.7005T>C MANE Select	ENSP00000384582.2:p.Asp2335=
ENST00000639431.1:c.265+16449T>C	ENSP00000491057.1:n.265+16449T>C
ENST00000639473.1:n.2464T>C
ENST00000640012.1:c.812T>C
ENST00000640374.1:n.149T>C
ENST00000640403.1:c.4296T>C	ENSP00000492531.1:p.Asp1432=
ENST00000640779.1:c.1734T>C
ENST00000405460.6:c.7005T>C	ENSP00000384582.2:p.Asp2335=
NM_032119.3:c.7005T>C	NP_115495.3:p.Asp2335=
NR_003149.1:n.7018T>C
XM_011543675.1:c.7002T>C	XP_011541977.1:p.Asp2334=
XM_011543676.1:c.6924T>C	XP_011541978.1:p.Asp2308=
XM_011543677.1:c.4308T>C	XP_011541979.1:p.Asp1436=
XM_011543678.1:c.7005T>C	XP_011541980.1:p.Asp2335=
XM_011543679.1:c.7005T>C	XP_011541981.1:p.Asp2335=
NM_032119.4:c.7005T>C MANE Select	NP_115495.3:p.Asp2335=
XM_017009963.2:c.7005T>C	XP_016865452.1:p.Asp2335=
XM_017009964.2:c.7002T>C	XP_016865453.1:p.Asp2334=
XM_017009965.1:c.7002T>C	XP_016865454.1:p.Asp2334=
XM_017009966.2:c.6924T>C	XP_016865455.1:p.Asp2308=
XM_017009967.1:c.6909T>C	XP_016865456.1:p.Asp2303=
XM_017009968.2:c.7005T>C	XP_016865457.1:p.Asp2335=
XM_017009969.2:c.7005T>C	XP_016865458.1:p.Asp2335=
XM_017009970.2:c.7005T>C	XP_016865459.1:p.Asp2335=
XM_017009971.2:c.7005T>C	XP_016865460.1:p.Asp2335=
XM_017009972.1:c.123T>C	XP_016865461.1:p.Asp41=
XM_017009973.1:c.123T>C	XP_016865462.1:p.Asp41=
XM_017009974.2:c.7005T>C	XP_016865463.1:p.Asp2335=
NR_003149.2:n.7021T>C