Canonical Allele Identifier: CA360403341
Gene: ADGRV1 HGNC NCBI

Linked Data

gnomAD v4: 5-90725627-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90725627A>G , CM000667.2:g.90725627A>G GRCh38
NC_000005.9:g.90021444A>G , CM000667.1:g.90021444A>G GRCh37
NC_000005.8:g.90057200A>G NCBI36
NG_007083.1:g.171828A>G
NG_007083.2:g.201284A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.10132A>G MANE Select ENSP00000384582.2:p.Ser3378Gly
ENST00000639431.1:c.265+49418A>G ENSP00000491057.1:n.265+49418A>G
ENST00000640374.1:n.3276A>G
ENST00000640464.1:n.551A>G
ENST00000405460.6:c.10132A>G ENSP00000384582.2:p.Ser3378Gly
ENST00000509621.1:c.2829A>G
NM_032119.3:c.10132A>G NP_115495.3:p.Ser3378Gly
NR_003149.1:n.10145A>G
XM_011543675.1:c.10129A>G XP_011541977.1:p.Ser3377Gly
XM_011543676.1:c.10051A>G XP_011541978.1:p.Ser3351Gly
XM_011543677.1:c.7435A>G XP_011541979.1:p.Ser2479Gly
XM_011543678.1:c.10132A>G XP_011541980.1:p.Ser3378Gly
XM_011543679.1:c.10132A>G XP_011541981.1:p.Ser3378Gly
XR_948560.1:n.272-9818T>C
NM_032119.4:c.10132A>G MANE Select NP_115495.3:p.Ser3378Gly
XM_017009963.2:c.10153A>G XP_016865452.1:p.Ser3385Gly
XM_017009964.2:c.10150A>G XP_016865453.1:p.Ser3384Gly
XM_017009965.1:c.10150A>G XP_016865454.1:p.Ser3384Gly
XM_017009966.2:c.10072A>G XP_016865455.1:p.Ser3358Gly
XM_017009967.1:c.10057A>G XP_016865456.1:p.Ser3353Gly
XM_017009968.2:c.10153A>G XP_016865457.1:p.Ser3385Gly
XM_017009969.2:c.10153A>G XP_016865458.1:p.Ser3385Gly
XM_017009970.2:c.10153A>G XP_016865459.1:p.Ser3385Gly
XM_017009971.2:c.10153A>G XP_016865460.1:p.Ser3385Gly
XM_017009972.1:c.3271A>G XP_016865461.1:p.Ser1091Gly
XM_017009973.1:c.3250A>G XP_016865462.1:p.Ser1084Gly
XM_017009974.2:c.10153A>G XP_016865463.1:p.Ser3385Gly
XR_001742802.1:n.2523-9818T>C
NR_003149.2:n.10148A>G