Canonical Allele Identifier: CA445406626
Gene: ADGRV1 HGNC NCBI

Linked Data

gnomAD v4: 5-90617812-A-G
MyVariant Identifiers: chr5:g.89913629A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90617812A>G , CM000667.2:g.90617812A>G GRCh38
NC_000005.9:g.89913629A>G , CM000667.1:g.89913629A>G GRCh37
NC_000005.8:g.89949385A>G NCBI36
NG_007083.1:g.64013A>G
NG_007083.2:g.93469A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.216A>G MANE Select ENSP00000384582.2:p.Gly72=
ENST00000638316.1:n.426A>G
ENST00000638638.1:n.623A>G
ENST00000640109.1:n.312A>G
ENST00000640281.1:n.275A>G
ENST00000405460.6:c.216A>G ENSP00000384582.2:p.Gly72=
ENST00000508842.5:c.228A>G ENSP00000425936.1:p.Gly76=
NM_032119.3:c.216A>G NP_115495.3:p.Gly72=
NR_003149.1:n.312A>G
XM_011543675.1:c.216A>G XP_011541977.1:p.Gly72=
XM_011543676.1:c.216A>G XP_011541978.1:p.Gly72=
XM_011543678.1:c.216A>G XP_011541980.1:p.Gly72=
XM_011543679.1:c.216A>G XP_011541981.1:p.Gly72=
NM_032119.4:c.216A>G MANE Select NP_115495.3:p.Gly72=
XM_017009963.2:c.216A>G XP_016865452.1:p.Gly72=
XM_017009964.2:c.216A>G XP_016865453.1:p.Gly72=
XM_017009965.1:c.213A>G XP_016865454.1:p.Gly71=
XM_017009966.2:c.216A>G XP_016865455.1:p.Gly72=
XM_017009967.1:c.216A>G XP_016865456.1:p.Gly72=
XM_017009968.2:c.216A>G XP_016865457.1:p.Gly72=
XM_017009969.2:c.216A>G XP_016865458.1:p.Gly72=
XM_017009970.2:c.216A>G XP_016865459.1:p.Gly72=
XM_017009971.2:c.216A>G XP_016865460.1:p.Gly72=
XM_017009974.2:c.216A>G XP_016865463.1:p.Gly72=
NR_003149.2:n.315A>G