Canonical Allele Identifier: CA2674581228

Gene: ADGRV1

Linked Data

• ClinVar Variation Id: 2861135
• ClinVar RCV Id: RCV003697234
• gnomAD v4: 5-90965403-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90965403T>C , CM000667.2:g.90965403T>C	GRCh38
NC_000005.9:g.90261220T>C , CM000667.1:g.90261220T>C	GRCh37
NC_000005.8:g.90296976T>C	NCBI36
NG_007083.1:g.411604T>C
NG_007083.2:g.441060T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.17857-12T>C MANE Select	ENSP00000384582.2:n.17857-12T>C
ENST00000425867.3:c.6811-12T>C	ENSP00000392618.3:n.6811-12T>C
ENST00000638510.1:n.5124-12T>C
ENST00000638990.1:c.1069-12T>C
ENST00000639431.1:c.266-19941T>C	ENSP00000491057.1:n.266-19941T>C
ENST00000639707.1:c.-60-12T>C	ENSP00000492328.1:n.-60-12T>C
ENST00000639821.1:c.-60-12T>C	ENSP00000492216.1:n.-60-12T>C
ENST00000640369.1:c.-60-12T>C	ENSP00000491401.1:n.-60-12T>C
ENST00000640407.1:c.4306-12T>C	ENSP00000491425.1:n.4306-12T>C
ENST00000640815.1:c.-60-12T>C	ENSP00000491767.1:n.-60-12T>C
ENST00000405460.6:c.17857-12T>C	ENSP00000384582.2:n.17857-12T>C
ENST00000425867.2:c.4840-12T>C	ENSP00000392618.2:n.4840-12T>C
NM_032119.3:c.17857-12T>C	NP_115495.3:n.17857-12T>C
NR_003149.1:n.17870-12T>C
XM_011543675.1:c.17854-12T>C	XP_011541977.1:n.17854-12T>C
XM_011543676.1:c.17776-12T>C	XP_011541978.1:n.17776-12T>C
XM_011543677.1:c.15160-12T>C	XP_011541979.1:n.15160-12T>C
NM_032119.4:c.17857-12T>C MANE Select	NP_115495.3:n.17857-12T>C
XM_017009963.2:c.17878-12T>C	XP_016865452.1:n.17878-12T>C
XM_017009964.2:c.17875-12T>C	XP_016865453.1:n.17875-12T>C
XM_017009965.1:c.17875-12T>C	XP_016865454.1:n.17875-12T>C
XM_017009966.2:c.17797-12T>C	XP_016865455.1:n.17797-12T>C
XM_017009967.1:c.17782-12T>C	XP_016865456.1:n.17782-12T>C
XM_017009968.2:c.17698-12T>C	XP_016865457.1:n.17698-12T>C
XM_017009969.2:c.17878-12T>C	XP_016865458.1:n.17878-12T>C
XM_017009972.1:c.10996-12T>C	XP_016865461.1:n.10996-12T>C
XM_017009973.1:c.10975-12T>C	XP_016865462.1:n.10975-12T>C
NR_003149.2:n.17873-12T>C