Canonical Allele Identifier: CA360403218
Gene: ADGRV1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90725575T>A , CM000667.2:g.90725575T>A GRCh38
NC_000005.9:g.90021392T>A , CM000667.1:g.90021392T>A GRCh37
NC_000005.8:g.90057148T>A NCBI36
NG_007083.1:g.171776T>A
NG_007083.2:g.201232T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.10080T>A MANE Select ENSP00000384582.2:p.Ser3360Arg
ENST00000639431.1:c.265+49366T>A ENSP00000491057.1:n.265+49366T>A
ENST00000640374.1:n.3224T>A
ENST00000640464.1:n.499T>A
ENST00000405460.6:c.10080T>A ENSP00000384582.2:p.Ser3360Arg
ENST00000509621.1:c.2777T>A
NM_032119.3:c.10080T>A NP_115495.3:p.Ser3360Arg
NR_003149.1:n.10093T>A
XM_011543675.1:c.10077T>A XP_011541977.1:p.Ser3359Arg
XM_011543676.1:c.9999T>A XP_011541978.1:p.Ser3333Arg
XM_011543677.1:c.7383T>A XP_011541979.1:p.Ser2461Arg
XM_011543678.1:c.10080T>A XP_011541980.1:p.Ser3360Arg
XM_011543679.1:c.10080T>A XP_011541981.1:p.Ser3360Arg
XR_948560.1:n.272-9766A>T
NM_032119.4:c.10080T>A MANE Select NP_115495.3:p.Ser3360Arg
XM_017009963.2:c.10101T>A XP_016865452.1:p.Ser3367Arg
XM_017009964.2:c.10098T>A XP_016865453.1:p.Ser3366Arg
XM_017009965.1:c.10098T>A XP_016865454.1:p.Ser3366Arg
XM_017009966.2:c.10020T>A XP_016865455.1:p.Ser3340Arg
XM_017009967.1:c.10005T>A XP_016865456.1:p.Ser3335Arg
XM_017009968.2:c.10101T>A XP_016865457.1:p.Ser3367Arg
XM_017009969.2:c.10101T>A XP_016865458.1:p.Ser3367Arg
XM_017009970.2:c.10101T>A XP_016865459.1:p.Ser3367Arg
XM_017009971.2:c.10101T>A XP_016865460.1:p.Ser3367Arg
XM_017009972.1:c.3219T>A XP_016865461.1:p.Ser1073Arg
XM_017009973.1:c.3198T>A XP_016865462.1:p.Ser1066Arg
XM_017009974.2:c.10101T>A XP_016865463.1:p.Ser3367Arg
XR_001742802.1:n.2523-9766A>T
NR_003149.2:n.10096T>A