Canonical Allele Identifier: CA445403701

Gene: ADGRV1

Linked Data

• ClinVar Variation Id: 2874537
• ClinVar RCV Id: RCV003714554
• dbSNP Id: rs1259842291
• gnomAD v2: 5-89918434-T-C
• gnomAD v4: 5-90622617-T-C
• MyVariant Identifiers: chr5:g.89918434T>C (hg19) ; chr5:g.90622617T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90622617T>C , CM000667.2:g.90622617T>C	GRCh38
NC_000005.9:g.89918434T>C , CM000667.1:g.89918434T>C	GRCh37
NC_000005.8:g.89954190T>C	NCBI36
NG_007083.1:g.68818T>C
NG_007083.2:g.98274T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.474T>C MANE Select	ENSP00000384582.2:p.Ser158=
ENST00000638316.1:n.684T>C
ENST00000638638.1:n.881T>C
ENST00000640083.1:n.179T>C
ENST00000640109.1:n.570T>C
ENST00000640281.1:n.533T>C
ENST00000405460.6:c.474T>C	ENSP00000384582.2:p.Ser158=
ENST00000508842.5:c.390T>C	ENSP00000425936.1:p.Ser130=
NM_032119.3:c.474T>C	NP_115495.3:p.Ser158=
NR_003149.1:n.570T>C
XM_011543675.1:c.474T>C	XP_011541977.1:p.Ser158=
XM_011543676.1:c.474T>C	XP_011541978.1:p.Ser158=
XM_011543678.1:c.474T>C	XP_011541980.1:p.Ser158=
XM_011543679.1:c.474T>C	XP_011541981.1:p.Ser158=
NM_032119.4:c.474T>C MANE Select	NP_115495.3:p.Ser158=
XM_017009963.2:c.474T>C	XP_016865452.1:p.Ser158=
XM_017009964.2:c.474T>C	XP_016865453.1:p.Ser158=
XM_017009965.1:c.471T>C	XP_016865454.1:p.Ser157=
XM_017009966.2:c.474T>C	XP_016865455.1:p.Ser158=
XM_017009967.1:c.378T>C	XP_016865456.1:p.Ser126=
XM_017009968.2:c.474T>C	XP_016865457.1:p.Ser158=
XM_017009969.2:c.474T>C	XP_016865458.1:p.Ser158=
XM_017009970.2:c.474T>C	XP_016865459.1:p.Ser158=
XM_017009971.2:c.474T>C	XP_016865460.1:p.Ser158=
XM_017009974.2:c.474T>C	XP_016865463.1:p.Ser158=
NR_003149.2:n.573T>C