Canonical Allele Identifier: CA360407497
Community Standard Title: NM_032119.4(ADGRV1):c.10570C>T (p.Gln3524Ter)
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90745066C>T , CM000667.2:g.90745066C>T GRCh38
NC_000005.9:g.90040883C>T , CM000667.1:g.90040883C>T GRCh37
NC_000005.8:g.90076639C>T NCBI36
NG_007083.1:g.191267C>T
NG_007083.2:g.220723C>T

Transcript Alleles

HGVS Amino-acid Change
NM_032119.4:c.10570C>T MANE Select NP_115495.3:p.Gln3524Ter
ENST00000405460.9:c.10570C>T MANE Select ENSP00000384582.2:p.Gln3524Ter
NM_032119.3:c.10570C>T NP_115495.3:p.Gln3524Ter
NR_003149.1:n.10583C>T
NR_003149.2:n.10586C>T
ENST00000405460.6:c.10570C>T ENSP00000384582.2:p.Gln3524Ter
ENST00000509621.1:c.3267C>T
ENST00000639431.1:c.265+68857C>T ENSP00000491057.1:n.265+68857C>T
ENST00000640374.1:n.3714C>T
ENST00000640464.1:n.989C>T
XM_011543675.1:c.10567C>T XP_011541977.1:p.Gln3523Ter
XM_011543676.1:c.10489C>T XP_011541978.1:p.Gln3497Ter
XM_011543677.1:c.7873C>T XP_011541979.1:p.Gln2625Ter
XM_011543678.1:c.10570C>T XP_011541980.1:p.Gln3524Ter
XM_011543679.1:c.10570C>T XP_011541981.1:p.Gln3524Ter
XM_017009963.2:c.10591C>T XP_016865452.1:p.Gln3531Ter
XM_017009964.2:c.10588C>T XP_016865453.1:p.Gln3530Ter
XM_017009965.1:c.10588C>T XP_016865454.1:p.Gln3530Ter
XM_017009966.2:c.10510C>T XP_016865455.1:p.Gln3504Ter
XM_017009967.1:c.10495C>T XP_016865456.1:p.Gln3499Ter
XM_017009968.2:c.10591C>T XP_016865457.1:p.Gln3531Ter
XM_017009969.2:c.10591C>T XP_016865458.1:p.Gln3531Ter
XM_017009970.2:c.10591C>T XP_016865459.1:p.Gln3531Ter
XM_017009971.2:c.10591C>T XP_016865460.1:p.Gln3531Ter
XM_017009972.1:c.3709C>T XP_016865461.1:p.Gln1237Ter
XM_017009973.1:c.3688C>T XP_016865462.1:p.Gln1230Ter
XM_017009974.2:c.10591C>T XP_016865463.1:p.Gln3531Ter