Canonical Allele Identifier: CA360401277
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90791107C>G , CM000667.2:g.90791107C>G GRCh38
NC_000005.9:g.90086924C>G , CM000667.1:g.90086924C>G GRCh37
NC_000005.8:g.90122680C>G NCBI36
NG_007083.1:g.237308C>G
NG_007083.2:g.266764C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.14278C>G MANE Select ENSP00000384582.2:p.Pro4760Ala
ENST00000425867.3:c.3232C>G ENSP00000392618.3:p.Pro1078Ala
ENST00000638510.1:n.1545C>G
ENST00000638585.1:n.44C>G
ENST00000638975.1:c.907C>G ENSP00000492630.1:p.Pro303Ala
ENST00000639431.1:c.265+114898C>G ENSP00000491057.1:n.265+114898C>G
ENST00000640407.1:c.688C>G ENSP00000491425.1:p.Pro230Ala
ENST00000405460.6:c.14278C>G ENSP00000384582.2:p.Pro4760Ala
ENST00000425867.2:c.1261C>G ENSP00000392618.2:p.Pro421Ala
NM_032119.3:c.14278C>G NP_115495.3:p.Pro4760Ala
NR_003149.1:n.14291C>G
XM_011543675.1:c.14275C>G XP_011541977.1:p.Pro4759Ala
XM_011543676.1:c.14197C>G XP_011541978.1:p.Pro4733Ala
XM_011543677.1:c.11581C>G XP_011541979.1:p.Pro3861Ala
XM_011543678.1:c.14278C>G XP_011541980.1:p.Pro4760Ala
NM_032119.4:c.14278C>G MANE Select NP_115495.3:p.Pro4760Ala
XM_017009963.2:c.14299C>G XP_016865452.1:p.Pro4767Ala
XM_017009964.2:c.14296C>G XP_016865453.1:p.Pro4766Ala
XM_017009965.1:c.14296C>G XP_016865454.1:p.Pro4766Ala
XM_017009966.2:c.14218C>G XP_016865455.1:p.Pro4740Ala
XM_017009967.1:c.14203C>G XP_016865456.1:p.Pro4735Ala
XM_017009968.2:c.14299C>G XP_016865457.1:p.Pro4767Ala
XM_017009969.2:c.14299C>G XP_016865458.1:p.Pro4767Ala
XM_017009970.2:c.14299C>G XP_016865459.1:p.Pro4767Ala
XM_017009971.2:c.14299C>G XP_016865460.1:p.Pro4767Ala
XM_017009972.1:c.7417C>G XP_016865461.1:p.Pro2473Ala
XM_017009973.1:c.7396C>G XP_016865462.1:p.Pro2466Ala
NR_003149.2:n.14294C>G