Canonical Allele Identifier: CA360397561
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90716653T>A , CM000667.2:g.90716653T>A GRCh38
NC_000005.9:g.90012470T>A , CM000667.1:g.90012470T>A GRCh37
NC_000005.8:g.90048226T>A NCBI36
NG_007083.1:g.162854T>A
NG_007083.2:g.192310T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.9371T>A MANE Select ENSP00000384582.2:p.Val3124Glu
ENST00000639431.1:c.265+40444T>A ENSP00000491057.1:n.265+40444T>A
ENST00000639473.1:n.4830T>A
ENST00000640012.1:c.3178T>A
ENST00000640374.1:n.2515T>A
ENST00000640779.1:c.4100T>A
ENST00000405460.6:c.9371T>A ENSP00000384582.2:p.Val3124Glu
ENST00000509621.1:c.2068T>A
NM_032119.3:c.9371T>A NP_115495.3:p.Val3124Glu
NR_003149.1:n.9384T>A
XM_011543675.1:c.9368T>A XP_011541977.1:p.Val3123Glu
XM_011543676.1:c.9290T>A XP_011541978.1:p.Val3097Glu
XM_011543677.1:c.6674T>A XP_011541979.1:p.Val2225Glu
XM_011543678.1:c.9371T>A XP_011541980.1:p.Val3124Glu
XM_011543679.1:c.9371T>A XP_011541981.1:p.Val3124Glu
XR_948560.1:n.272-844A>T
NM_032119.4:c.9371T>A MANE Select NP_115495.3:p.Val3124Glu
XM_017009963.2:c.9392T>A XP_016865452.1:p.Val3131Glu
XM_017009964.2:c.9389T>A XP_016865453.1:p.Val3130Glu
XM_017009965.1:c.9389T>A XP_016865454.1:p.Val3130Glu
XM_017009966.2:c.9311T>A XP_016865455.1:p.Val3104Glu
XM_017009967.1:c.9296T>A XP_016865456.1:p.Val3099Glu
XM_017009968.2:c.9392T>A XP_016865457.1:p.Val3131Glu
XM_017009969.2:c.9392T>A XP_016865458.1:p.Val3131Glu
XM_017009970.2:c.9392T>A XP_016865459.1:p.Val3131Glu
XM_017009971.2:c.9392T>A XP_016865460.1:p.Val3131Glu
XM_017009972.1:c.2510T>A XP_016865461.1:p.Val837Glu
XM_017009973.1:c.2489T>A XP_016865462.1:p.Val830Glu
XM_017009974.2:c.9392T>A XP_016865463.1:p.Val3131Glu
XR_001742802.1:n.2523-844A>T
NR_003149.2:n.9387T>A