Canonical Allele Identifier: CA360396245
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90712345A>C , CM000667.2:g.90712345A>C GRCh38
NC_000005.9:g.90008162A>C , CM000667.1:g.90008162A>C GRCh37
NC_000005.8:g.90043918A>C NCBI36
NG_007083.1:g.158546A>C
NG_007083.2:g.188002A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.9101A>C MANE Select ENSP00000384582.2:p.Asp3034Ala
ENST00000639431.1:c.265+36136A>C ENSP00000491057.1:n.265+36136A>C
ENST00000639473.1:n.4560A>C
ENST00000640012.1:c.2908A>C
ENST00000640374.1:n.2245A>C
ENST00000640779.1:c.3830A>C
ENST00000405460.6:c.9101A>C ENSP00000384582.2:p.Asp3034Ala
ENST00000509621.1:c.1798A>C
NM_032119.3:c.9101A>C NP_115495.3:p.Asp3034Ala
NR_003149.1:n.9114A>C
XM_011543675.1:c.9098A>C XP_011541977.1:p.Asp3033Ala
XM_011543676.1:c.9020A>C XP_011541978.1:p.Asp3007Ala
XM_011543677.1:c.6404A>C XP_011541979.1:p.Asp2135Ala
XM_011543678.1:c.9101A>C XP_011541980.1:p.Asp3034Ala
XM_011543679.1:c.9101A>C XP_011541981.1:p.Asp3034Ala
NM_032119.4:c.9101A>C MANE Select NP_115495.3:p.Asp3034Ala
XM_017009963.2:c.9122A>C XP_016865452.1:p.Asp3041Ala
XM_017009964.2:c.9119A>C XP_016865453.1:p.Asp3040Ala
XM_017009965.1:c.9119A>C XP_016865454.1:p.Asp3040Ala
XM_017009966.2:c.9041A>C XP_016865455.1:p.Asp3014Ala
XM_017009967.1:c.9026A>C XP_016865456.1:p.Asp3009Ala
XM_017009968.2:c.9122A>C XP_016865457.1:p.Asp3041Ala
XM_017009969.2:c.9122A>C XP_016865458.1:p.Asp3041Ala
XM_017009970.2:c.9122A>C XP_016865459.1:p.Asp3041Ala
XM_017009971.2:c.9122A>C XP_016865460.1:p.Asp3041Ala
XM_017009972.1:c.2240A>C XP_016865461.1:p.Asp747Ala
XM_017009973.1:c.2219A>C XP_016865462.1:p.Asp740Ala
XM_017009974.2:c.9122A>C XP_016865463.1:p.Asp3041Ala
NR_003149.2:n.9117A>C