Canonical Allele Identifier: CA3338560
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs753757818
gnomAD v2: 5-89923110-T-A
gnomAD v3: 5-90627293-T-A
gnomAD v4: 5-90627293-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90627293T>A , CM000667.2:g.90627293T>A GRCh38
NC_000005.9:g.89923110T>A , CM000667.1:g.89923110T>A GRCh37
NC_000005.8:g.89958866T>A NCBI36
NG_007083.1:g.73494T>A
NG_007083.2:g.102950T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.755T>A MANE Select ENSP00000384582.2:p.Ile252Asn
ENST00000640083.1:n.460T>A
ENST00000640109.1:n.851T>A
ENST00000640281.1:n.814T>A
ENST00000405460.6:c.755T>A ENSP00000384582.2:p.Ile252Asn
NM_032119.3:c.755T>A NP_115495.3:p.Ile252Asn
NR_003149.1:n.851T>A
XM_011543675.1:c.755T>A XP_011541977.1:p.Ile252Asn
XM_011543676.1:c.755T>A XP_011541978.1:p.Ile252Asn
XM_011543678.1:c.755T>A XP_011541980.1:p.Ile252Asn
XM_011543679.1:c.755T>A XP_011541981.1:p.Ile252Asn
NM_032119.4:c.755T>A MANE Select NP_115495.3:p.Ile252Asn
XM_017009963.2:c.755T>A XP_016865452.1:p.Ile252Asn
XM_017009964.2:c.755T>A XP_016865453.1:p.Ile252Asn
XM_017009965.1:c.752T>A XP_016865454.1:p.Ile251Asn
XM_017009966.2:c.755T>A XP_016865455.1:p.Ile252Asn
XM_017009967.1:c.659T>A XP_016865456.1:p.Ile220Asn
XM_017009968.2:c.755T>A XP_016865457.1:p.Ile252Asn
XM_017009969.2:c.755T>A XP_016865458.1:p.Ile252Asn
XM_017009970.2:c.755T>A XP_016865459.1:p.Ile252Asn
XM_017009971.2:c.755T>A XP_016865460.1:p.Ile252Asn
XM_017009974.2:c.755T>A XP_016865463.1:p.Ile252Asn
NR_003149.2:n.854T>A