Canonical Allele Identifier: CA360403420
Community Standard Title: NM_032119.4(ADGRV1):c.4379-1G>A
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90657904G>A , CM000667.2:g.90657904G>A GRCh38
NC_000005.9:g.89953721G>A , CM000667.1:g.89953721G>A GRCh37
NC_000005.8:g.89989477G>A NCBI36
NG_007083.1:g.104105G>A
NG_007083.2:g.133561G>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.4379-1G>A MANE Select NP_115495.3:n.4379-1G>A
ENST00000405460.9:c.4379-1G>A MANE Select ENSP00000384582.2:n.4379-1G>A
NM_032119.3:c.4379-1G>A NP_115495.3:n.4379-1G>A
NR_003149.1:n.4475-1G>A
NR_003149.2:n.4478-1G>A
ENST00000405460.6:c.4379-1G>A ENSP00000384582.2:n.4379-1G>A
ENST00000639676.1:n.1977-1G>A
ENST00000640403.1:c.1670-1G>A ENSP00000492531.1:n.1670-1G>A
XM_011543675.1:c.4379-1G>A XP_011541977.1:n.4379-1G>A
XM_011543676.1:c.4379-1G>A XP_011541978.1:n.4379-1G>A
XM_011543677.1:c.1682-1G>A XP_011541979.1:n.1682-1G>A
XM_011543678.1:c.4379-1G>A XP_011541980.1:n.4379-1G>A
XM_011543679.1:c.4379-1G>A XP_011541981.1:n.4379-1G>A
XM_017009963.2:c.4379-1G>A XP_016865452.1:n.4379-1G>A
XM_017009964.2:c.4379-1G>A XP_016865453.1:n.4379-1G>A
XM_017009965.1:c.4376-1G>A XP_016865454.1:n.4376-1G>A
XM_017009966.2:c.4379-1G>A XP_016865455.1:n.4379-1G>A
XM_017009967.1:c.4283-1G>A XP_016865456.1:n.4283-1G>A
XM_017009968.2:c.4379-1G>A XP_016865457.1:n.4379-1G>A
XM_017009969.2:c.4379-1G>A XP_016865458.1:n.4379-1G>A
XM_017009970.2:c.4379-1G>A XP_016865459.1:n.4379-1G>A
XM_017009971.2:c.4379-1G>A XP_016865460.1:n.4379-1G>A
XM_017009974.2:c.4379-1G>A XP_016865463.1:n.4379-1G>A