Canonical Allele Identifier: CA360396315
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90712375A>C , CM000667.2:g.90712375A>C GRCh38
NC_000005.9:g.90008192A>C , CM000667.1:g.90008192A>C GRCh37
NC_000005.8:g.90043948A>C NCBI36
NG_007083.1:g.158576A>C
NG_007083.2:g.188032A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.9131A>C MANE Select ENSP00000384582.2:p.Gln3044Pro
ENST00000639431.1:c.265+36166A>C ENSP00000491057.1:n.265+36166A>C
ENST00000639473.1:n.4590A>C
ENST00000640012.1:c.2938A>C
ENST00000640374.1:n.2275A>C
ENST00000640779.1:c.3860A>C
ENST00000405460.6:c.9131A>C ENSP00000384582.2:p.Gln3044Pro
ENST00000509621.1:c.1828A>C
NM_032119.3:c.9131A>C NP_115495.3:p.Gln3044Pro
NR_003149.1:n.9144A>C
XM_011543675.1:c.9128A>C XP_011541977.1:p.Gln3043Pro
XM_011543676.1:c.9050A>C XP_011541978.1:p.Gln3017Pro
XM_011543677.1:c.6434A>C XP_011541979.1:p.Gln2145Pro
XM_011543678.1:c.9131A>C XP_011541980.1:p.Gln3044Pro
XM_011543679.1:c.9131A>C XP_011541981.1:p.Gln3044Pro
NM_032119.4:c.9131A>C MANE Select NP_115495.3:p.Gln3044Pro
XM_017009963.2:c.9152A>C XP_016865452.1:p.Gln3051Pro
XM_017009964.2:c.9149A>C XP_016865453.1:p.Gln3050Pro
XM_017009965.1:c.9149A>C XP_016865454.1:p.Gln3050Pro
XM_017009966.2:c.9071A>C XP_016865455.1:p.Gln3024Pro
XM_017009967.1:c.9056A>C XP_016865456.1:p.Gln3019Pro
XM_017009968.2:c.9152A>C XP_016865457.1:p.Gln3051Pro
XM_017009969.2:c.9152A>C XP_016865458.1:p.Gln3051Pro
XM_017009970.2:c.9152A>C XP_016865459.1:p.Gln3051Pro
XM_017009971.2:c.9152A>C XP_016865460.1:p.Gln3051Pro
XM_017009972.1:c.2270A>C XP_016865461.1:p.Gln757Pro
XM_017009973.1:c.2249A>C XP_016865462.1:p.Gln750Pro
XM_017009974.2:c.9152A>C XP_016865463.1:p.Gln3051Pro
NR_003149.2:n.9147A>C