Canonical Allele Identifier: CA815371025

Gene: ADGRV1

Linked Data

• dbSNP Id: rs1208833756
• gnomAD v3: 5-90914002-T-A
• gnomAD v4: 5-90914002-T-A
• MyVariant Identifiers: chr5:g.90209819T>A (hg19) ; chr5:g.90914002T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90914002T>A , CM000667.2:g.90914002T>A	GRCh38
NC_000005.9:g.90209819T>A , CM000667.1:g.90209819T>A	GRCh37
NC_000005.8:g.90245575T>A	NCBI36
NG_007083.1:g.360203T>A
NG_007083.2:g.389659T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000405460.9:c.17856+50145T>A MANE Select	ENSP00000384582.2:n.17856+50145T>A
ENST00000425867.3:c.6810+50145T>A	ENSP00000392618.3:n.6810+50145T>A
ENST00000638510.1:n.5123+50145T>A
ENST00000638990.1:c.1068+50145T>A
ENST00000639431.1:c.266-71342T>A	ENSP00000491057.1:n.266-71342T>A
ENST00000640407.1:c.4305+50145T>A	ENSP00000491425.1:n.4305+50145T>A
ENST00000640815.1:c.-61+14679T>A	ENSP00000491767.1:n.-61+14679T>A
ENST00000405460.6:c.17856+50145T>A	ENSP00000384582.2:n.17856+50145T>A
ENST00000425867.2:c.4839+50145T>A	ENSP00000392618.2:n.4839+50145T>A
NM_032119.3:c.17856+50145T>A	NP_115495.3:n.17856+50145T>A
NR_003149.1:n.17869+50145T>A
XM_011543675.1:c.17853+50145T>A	XP_011541977.1:n.17853+50145T>A
XM_011543676.1:c.17775+50145T>A	XP_011541978.1:n.17775+50145T>A
XM_011543677.1:c.15159+50145T>A	XP_011541979.1:n.15159+50145T>A
NM_032119.4:c.17856+50145T>A MANE Select	NP_115495.3:n.17856+50145T>A
XM_017009963.2:c.17877+50145T>A	XP_016865452.1:n.17877+50145T>A
XM_017009964.2:c.17874+50145T>A	XP_016865453.1:n.17874+50145T>A
XM_017009965.1:c.17874+50145T>A	XP_016865454.1:n.17874+50145T>A
XM_017009966.2:c.17796+50145T>A	XP_016865455.1:n.17796+50145T>A
XM_017009967.1:c.17781+50145T>A	XP_016865456.1:n.17781+50145T>A
XM_017009968.2:c.17697+50145T>A	XP_016865457.1:n.17697+50145T>A
XM_017009969.2:c.17877+50145T>A	XP_016865458.1:n.17877+50145T>A
XM_017009972.1:c.10995+50145T>A	XP_016865461.1:n.10995+50145T>A
XM_017009973.1:c.10974+50145T>A	XP_016865462.1:n.10974+50145T>A
NR_003149.2:n.17872+50145T>A