Canonical Allele Identifier: CA360431127
Community Standard Title: NM_032119.4(ADGRV1):c.17763C>A (p.Cys5921Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90863764C>A , CM000667.2:g.90863764C>A GRCh38
NC_000005.9:g.90159581C>A , CM000667.1:g.90159581C>A GRCh37
NC_000005.8:g.90195337C>A NCBI36
NG_007083.1:g.309965C>A
NG_007083.2:g.339421C>A

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.17763C>A MANE Select NP_115495.3:p.Cys5921Ter
ENST00000405460.9:c.17763C>A MANE Select ENSP00000384582.2:p.Cys5921Ter
NM_032119.3:c.17763C>A NP_115495.3:p.Cys5921Ter
NR_003149.1:n.17776C>A
NR_003149.2:n.17779C>A
ENST00000405460.6:c.17763C>A ENSP00000384582.2:p.Cys5921Ter
ENST00000425867.2:c.4746C>A ENSP00000392618.2:p.Cys1582Ter
ENST00000425867.3:c.6717C>A ENSP00000392618.3:p.Cys2239Ter
ENST00000503852.1:n.311C>A
ENST00000638510.1:n.5030C>A
ENST00000638990.1:c.975C>A
ENST00000639431.1:c.266-121580C>A ENSP00000491057.1:n.266-121580C>A
ENST00000640407.1:c.4212C>A ENSP00000491425.1:n.4212C>A
XM_011543675.1:c.17760C>A XP_011541977.1:p.Cys5920Ter
XM_011543676.1:c.17682C>A XP_011541978.1:p.Cys5894Ter
XM_011543677.1:c.15066C>A XP_011541979.1:p.Cys5022Ter
XM_017009963.2:c.17784C>A XP_016865452.1:p.Cys5928Ter
XM_017009964.2:c.17781C>A XP_016865453.1:p.Cys5927Ter
XM_017009965.1:c.17781C>A XP_016865454.1:p.Cys5927Ter
XM_017009966.2:c.17703C>A XP_016865455.1:p.Cys5901Ter
XM_017009967.1:c.17688C>A XP_016865456.1:p.Cys5896Ter
XM_017009968.2:c.17604C>A XP_016865457.1:p.Cys5868Ter
XM_017009969.2:c.17784C>A XP_016865458.1:p.Cys5928Ter
XM_017009972.1:c.10902C>A XP_016865461.1:p.Cys3634Ter
XM_017009973.1:c.10881C>A XP_016865462.1:p.Cys3627Ter