Canonical Allele Identifier: CA1562882089
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90745670_90745673delinsAAAG , CM000667.2:g.90745670_90745673delinsAAAG GRCh38
NC_000005.9:g.90041487_90041490delinsAAAG , CM000667.1:g.90041487_90041490delinsAAAG GRCh37
NC_000005.8:g.90077243_90077246delinsAAAG NCBI36
NG_007083.1:g.191871_191874delinsAAAG
NG_007083.2:g.221327_221330delinsAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000405460.9:c.10849_10852delinsAAAG MANE Select ENSP00000384582.2:p.Lys3617=
ENST00000639431.1:c.265+69461_265+69464delinsAAAG ENSP00000491057.1:n.265+69461_265+69464delinsAAAG
ENST00000640374.1:n.3993_3996delinsAAAG
ENST00000640464.1:n.1268_1271delinsAAAG
ENST00000405460.6:c.10849_10852delinsAAAG ENSP00000384582.2:p.Lys3617=
ENST00000509621.1:c.3546_3549delinsAAAG
NM_032119.3:c.10849_10852delinsAAAG NP_115495.3:p.Lys3617=
NR_003149.1:n.10862_10865delinsAAAG
XM_011543675.1:c.10846_10849delinsAAAG XP_011541977.1:p.Lys3616=
XM_011543676.1:c.10768_10771delinsAAAG XP_011541978.1:p.Lys3590=
XM_011543677.1:c.8152_8155delinsAAAG XP_011541979.1:p.Lys2718=
XM_011543678.1:c.10849_10852delinsAAAG XP_011541980.1:p.Lys3617=
XM_011543679.1:c.*71_*74delinsAAAG XP_011541981.1:n.*71_*74delinsAAAG
NM_032119.4:c.10849_10852delinsAAAG MANE Select NP_115495.3:p.Lys3617=
XM_017009963.2:c.10870_10873delinsAAAG XP_016865452.1:p.Lys3624=
XM_017009964.2:c.10867_10870delinsAAAG XP_016865453.1:p.Lys3623=
XM_017009965.1:c.10867_10870delinsAAAG XP_016865454.1:p.Lys3623=
XM_017009966.2:c.10789_10792delinsAAAG XP_016865455.1:p.Lys3597=
XM_017009967.1:c.10774_10777delinsAAAG XP_016865456.1:p.Lys3592=
XM_017009968.2:c.10870_10873delinsAAAG XP_016865457.1:p.Lys3624=
XM_017009969.2:c.10870_10873delinsAAAG XP_016865458.1:p.Lys3624=
XM_017009970.2:c.10870_10873delinsAAAG XP_016865459.1:p.Lys3624=
XM_017009971.2:c.10870_10873delinsAAAG XP_016865460.1:p.Lys3624=
XM_017009972.1:c.3988_3991delinsAAAG XP_016865461.1:p.Lys1330=
XM_017009973.1:c.3967_3970delinsAAAG XP_016865462.1:p.Lys1323=
XM_017009974.2:c.*71_*74delinsAAAG XP_016865463.1:n.*71_*74delinsAAAG
NR_003149.2:n.10865_10868delinsAAAG