Canonical Allele Identifier: CA1562874980
Gene: ADGRV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.90728942_90728947delinsATAAAG , CM000667.2:g.90728942_90728947delinsATAAAG GRCh38
NC_000005.9:g.90024759_90024764delinsATAAAG , CM000667.1:g.90024759_90024764delinsATAAAG GRCh37
NC_000005.8:g.90060515_90060520delinsATAAAG NCBI36
NG_007083.1:g.175143_175148delinsATAAAG
NG_007083.2:g.204599_204604delinsATAAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000405460.9:c.10426+9_10426+14delinsATAAAG MANE Select ENSP00000384582.2:n.10426+9_10426+14delin...
ENST00000639431.1:c.265+52733_265+52738delinsATAAAG ENSP00000491057.1:n.265+52733_265+52738de...
ENST00000640374.1:n.3570+9_3570+14delinsATAAAG
ENST00000640464.1:n.845+9_845+14delinsATAAAG
ENST00000405460.6:c.10426+9_10426+14delinsATAAAG ENSP00000384582.2:n.10426+9_10426+14delin...
ENST00000509621.1:c.3123+9_3123+14delinsATAAAG
NM_032119.3:c.10426+9_10426+14delinsATAAAG NP_115495.3:n.10426+9_10426+14delinsATAAA...
NR_003149.1:n.10439+9_10439+14delinsATAAAG
XM_011543675.1:c.10423+9_10423+14delinsATAAAG XP_011541977.1:n.10423+9_10423+14delinsAT...
XM_011543676.1:c.10345+9_10345+14delinsATAAAG XP_011541978.1:n.10345+9_10345+14delinsAT...
XM_011543677.1:c.7729+9_7729+14delinsATAAAG XP_011541979.1:n.7729+9_7729+14delinsATAA...
XM_011543678.1:c.10426+9_10426+14delinsATAAAG XP_011541980.1:n.10426+9_10426+14delinsAT...
XM_011543679.1:c.10426+9_10426+14delinsATAAAG XP_011541981.1:n.10426+9_10426+14delinsAT...
XR_948560.1:n.271+11960_271+11965delinsCTTTAT
NM_032119.4:c.10426+9_10426+14delinsATAAAG MANE Select NP_115495.3:n.10426+9_10426+14delinsATAAA...
XM_017009963.2:c.10447+9_10447+14delinsATAAAG XP_016865452.1:n.10447+9_10447+14delinsAT...
XM_017009964.2:c.10444+9_10444+14delinsATAAAG XP_016865453.1:n.10444+9_10444+14delinsAT...
XM_017009965.1:c.10444+9_10444+14delinsATAAAG XP_016865454.1:n.10444+9_10444+14delinsAT...
XM_017009966.2:c.10366+9_10366+14delinsATAAAG XP_016865455.1:n.10366+9_10366+14delinsAT...
XM_017009967.1:c.10351+9_10351+14delinsATAAAG XP_016865456.1:n.10351+9_10351+14delinsAT...
XM_017009968.2:c.10447+9_10447+14delinsATAAAG XP_016865457.1:n.10447+9_10447+14delinsAT...
XM_017009969.2:c.10447+9_10447+14delinsATAAAG XP_016865458.1:n.10447+9_10447+14delinsAT...
XM_017009970.2:c.10447+9_10447+14delinsATAAAG XP_016865459.1:n.10447+9_10447+14delinsAT...
XM_017009971.2:c.10447+9_10447+14delinsATAAAG XP_016865460.1:n.10447+9_10447+14delinsAT...
XM_017009972.1:c.3565+9_3565+14delinsATAAAG XP_016865461.1:n.3565+9_3565+14delinsATAA...
XM_017009973.1:c.3544+9_3544+14delinsATAAAG XP_016865462.1:n.3544+9_3544+14delinsATAA...
XM_017009974.2:c.10447+9_10447+14delinsATAAAG XP_016865463.1:n.10447+9_10447+14delinsAT...
XR_001742802.1:n.2522+11960_2522+11965delinsCTTTAT
NR_003149.2:n.10442+9_10442+14delinsATAAAG