Canonical Allele Identifier: CA138102
Gene: ADGRV1 HGNC NCBI

Linked Data

ClinVar Variation Id: 46314
dbSNP Id: rs61753944
gnomAD v2: 5-89913740-C-T
gnomAD v3: 5-90617923-C-T
gnomAD v4: 5-90617923-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90617923C>T , CM000667.2:g.90617923C>T GRCh38
NC_000005.9:g.89913740C>T , CM000667.1:g.89913740C>T GRCh37
NC_000005.8:g.89949496C>T NCBI36
NG_007083.1:g.64124C>T
NG_007083.2:g.93580C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.327C>T MANE Select ENSP00000384582.2:p.Asp109=
ENST00000638316.1:n.537C>T
ENST00000638638.1:n.734C>T
ENST00000640083.1:n.32C>T
ENST00000640109.1:n.423C>T
ENST00000640281.1:n.386C>T
ENST00000405460.6:c.327C>T ENSP00000384582.2:p.Asp109=
ENST00000508842.5:c.339C>T ENSP00000425936.1:p.Asp113=
NM_032119.3:c.327C>T NP_115495.3:p.Asp109=
NR_003149.1:n.423C>T
XM_011543675.1:c.327C>T XP_011541977.1:p.Asp109=
XM_011543676.1:c.327C>T XP_011541978.1:p.Asp109=
XM_011543678.1:c.327C>T XP_011541980.1:p.Asp109=
XM_011543679.1:c.327C>T XP_011541981.1:p.Asp109=
NM_032119.4:c.327C>T MANE Select NP_115495.3:p.Asp109=
XM_017009963.2:c.327C>T XP_016865452.1:p.Asp109=
XM_017009964.2:c.327C>T XP_016865453.1:p.Asp109=
XM_017009965.1:c.324C>T XP_016865454.1:p.Asp108=
XM_017009966.2:c.327C>T XP_016865455.1:p.Asp109=
XM_017009967.1:c.327C>T XP_016865456.1:p.Asp109=
XM_017009968.2:c.327C>T XP_016865457.1:p.Asp109=
XM_017009969.2:c.327C>T XP_016865458.1:p.Asp109=
XM_017009970.2:c.327C>T XP_016865459.1:p.Asp109=
XM_017009971.2:c.327C>T XP_016865460.1:p.Asp109=
XM_017009974.2:c.327C>T XP_016865463.1:p.Asp109=
NR_003149.2:n.426C>T