Canonical Allele Identifier: CA360403250
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90725589A>G , CM000667.2:g.90725589A>G GRCh38
NC_000005.9:g.90021406A>G , CM000667.1:g.90021406A>G GRCh37
NC_000005.8:g.90057162A>G NCBI36
NG_007083.1:g.171790A>G
NG_007083.2:g.201246A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.10094A>G MANE Select ENSP00000384582.2:p.Tyr3365Cys
ENST00000639431.1:c.265+49380A>G ENSP00000491057.1:n.265+49380A>G
ENST00000640374.1:n.3238A>G
ENST00000640464.1:n.513A>G
ENST00000405460.6:c.10094A>G ENSP00000384582.2:p.Tyr3365Cys
ENST00000509621.1:c.2791A>G
NM_032119.3:c.10094A>G NP_115495.3:p.Tyr3365Cys
NR_003149.1:n.10107A>G
XM_011543675.1:c.10091A>G XP_011541977.1:p.Tyr3364Cys
XM_011543676.1:c.10013A>G XP_011541978.1:p.Tyr3338Cys
XM_011543677.1:c.7397A>G XP_011541979.1:p.Tyr2466Cys
XM_011543678.1:c.10094A>G XP_011541980.1:p.Tyr3365Cys
XM_011543679.1:c.10094A>G XP_011541981.1:p.Tyr3365Cys
XR_948560.1:n.272-9780T>C
NM_032119.4:c.10094A>G MANE Select NP_115495.3:p.Tyr3365Cys
XM_017009963.2:c.10115A>G XP_016865452.1:p.Tyr3372Cys
XM_017009964.2:c.10112A>G XP_016865453.1:p.Tyr3371Cys
XM_017009965.1:c.10112A>G XP_016865454.1:p.Tyr3371Cys
XM_017009966.2:c.10034A>G XP_016865455.1:p.Tyr3345Cys
XM_017009967.1:c.10019A>G XP_016865456.1:p.Tyr3340Cys
XM_017009968.2:c.10115A>G XP_016865457.1:p.Tyr3372Cys
XM_017009969.2:c.10115A>G XP_016865458.1:p.Tyr3372Cys
XM_017009970.2:c.10115A>G XP_016865459.1:p.Tyr3372Cys
XM_017009971.2:c.10115A>G XP_016865460.1:p.Tyr3372Cys
XM_017009972.1:c.3233A>G XP_016865461.1:p.Tyr1078Cys
XM_017009973.1:c.3212A>G XP_016865462.1:p.Tyr1071Cys
XM_017009974.2:c.10115A>G XP_016865463.1:p.Tyr3372Cys
XR_001742802.1:n.2523-9780T>C
NR_003149.2:n.10110A>G