Canonical Allele Identifier: CA122797178
Gene: ADGRV1 HGNC NCBI

Linked Data

dbSNP Id: rs936423636
gnomAD v2: 5-89988259-C-T
gnomAD v3: 5-90692442-C-T
gnomAD v4: 5-90692442-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90692442C>T , CM000667.2:g.90692442C>T GRCh38
NC_000005.9:g.89988259C>T , CM000667.1:g.89988259C>T GRCh37
NC_000005.8:g.90024015C>T NCBI36
NG_007083.1:g.138643C>T
NG_007083.2:g.168099C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.6952-163C>T MANE Select ENSP00000384582.2:n.6952-163C>T
ENST00000639431.1:c.265+16233C>T ENSP00000491057.1:n.265+16233C>T
ENST00000639473.1:n.2411-163C>T
ENST00000640012.1:c.759-163C>T
ENST00000640374.1:n.96-163C>T
ENST00000640403.1:c.4243-163C>T ENSP00000492531.1:n.4243-163C>T
ENST00000640779.1:c.1681-163C>T
ENST00000405460.6:c.6952-163C>T ENSP00000384582.2:n.6952-163C>T
NM_032119.3:c.6952-163C>T NP_115495.3:n.6952-163C>T
NR_003149.1:n.6965-163C>T
XM_011543675.1:c.6949-163C>T XP_011541977.1:n.6949-163C>T
XM_011543676.1:c.6871-163C>T XP_011541978.1:n.6871-163C>T
XM_011543677.1:c.4255-163C>T XP_011541979.1:n.4255-163C>T
XM_011543678.1:c.6952-163C>T XP_011541980.1:n.6952-163C>T
XM_011543679.1:c.6952-163C>T XP_011541981.1:n.6952-163C>T
NM_032119.4:c.6952-163C>T MANE Select NP_115495.3:n.6952-163C>T
XM_017009963.2:c.6952-163C>T XP_016865452.1:n.6952-163C>T
XM_017009964.2:c.6949-163C>T XP_016865453.1:n.6949-163C>T
XM_017009965.1:c.6949-163C>T XP_016865454.1:n.6949-163C>T
XM_017009966.2:c.6871-163C>T XP_016865455.1:n.6871-163C>T
XM_017009967.1:c.6856-163C>T XP_016865456.1:n.6856-163C>T
XM_017009968.2:c.6952-163C>T XP_016865457.1:n.6952-163C>T
XM_017009969.2:c.6952-163C>T XP_016865458.1:n.6952-163C>T
XM_017009970.2:c.6952-163C>T XP_016865459.1:n.6952-163C>T
XM_017009971.2:c.6952-163C>T XP_016865460.1:n.6952-163C>T
XM_017009972.1:c.70-163C>T XP_016865461.1:n.70-163C>T
XM_017009973.1:c.70-163C>T XP_016865462.1:n.70-163C>T
XM_017009974.2:c.6952-163C>T XP_016865463.1:n.6952-163C>T
NR_003149.2:n.6968-163C>T