Canonical Allele Identifier: CA2767421103

Gene: ADGRV1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90729080_90729081insAGTC , CM000667.2:g.90729080_90729081insAGTC	GRCh38
NC_000005.9:g.90024897_90024898insAGTC , CM000667.1:g.90024897_90024898insAGTC	GRCh37
NC_000005.8:g.90060653_90060654insAGTC	NCBI36
NG_007083.1:g.175281_175282insAGTC
NG_007083.2:g.204737_204738insAGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10426+147_10426+148insAGTC MANE Select	ENSP00000384582.2:n.10426+147_10426+148insAGTC
ENST00000639431.1:c.265+52871_265+52872insAGTC	ENSP00000491057.1:n.265+52871_265+52872insAGTC
ENST00000640374.1:n.3570+147_3570+148insAGTC
ENST00000640464.1:n.845+147_845+148insAGTC
ENST00000405460.6:c.10426+147_10426+148insAGTC	ENSP00000384582.2:n.10426+147_10426+148insAGTC
ENST00000509621.1:c.3123+147_3123+148insAGTC
NM_032119.3:c.10426+147_10426+148insAGTC	NP_115495.3:n.10426+147_10426+148insAGTC
NR_003149.1:n.10439+147_10439+148insAGTC
XM_011543675.1:c.10423+147_10423+148insAGTC	XP_011541977.1:n.10423+147_10423+148insAGTC
XM_011543676.1:c.10345+147_10345+148insAGTC	XP_011541978.1:n.10345+147_10345+148insAGTC
XM_011543677.1:c.7729+147_7729+148insAGTC	XP_011541979.1:n.7729+147_7729+148insAGTC
XM_011543678.1:c.10426+147_10426+148insAGTC	XP_011541980.1:n.10426+147_10426+148insAGTC
XM_011543679.1:c.10426+147_10426+148insAGTC	XP_011541981.1:n.10426+147_10426+148insAGTC
XR_948560.1:n.271+11826_271+11827insGACT
NM_032119.4:c.10426+147_10426+148insAGTC MANE Select	NP_115495.3:n.10426+147_10426+148insAGTC
XM_017009963.2:c.10447+147_10447+148insAGTC	XP_016865452.1:n.10447+147_10447+148insAGTC
XM_017009964.2:c.10444+147_10444+148insAGTC	XP_016865453.1:n.10444+147_10444+148insAGTC
XM_017009965.1:c.10444+147_10444+148insAGTC	XP_016865454.1:n.10444+147_10444+148insAGTC
XM_017009966.2:c.10366+147_10366+148insAGTC	XP_016865455.1:n.10366+147_10366+148insAGTC
XM_017009967.1:c.10351+147_10351+148insAGTC	XP_016865456.1:n.10351+147_10351+148insAGTC
XM_017009968.2:c.10447+147_10447+148insAGTC	XP_016865457.1:n.10447+147_10447+148insAGTC
XM_017009969.2:c.10447+147_10447+148insAGTC	XP_016865458.1:n.10447+147_10447+148insAGTC
XM_017009970.2:c.10447+147_10447+148insAGTC	XP_016865459.1:n.10447+147_10447+148insAGTC
XM_017009971.2:c.10447+147_10447+148insAGTC	XP_016865460.1:n.10447+147_10447+148insAGTC
XM_017009972.1:c.3565+147_3565+148insAGTC	XP_016865461.1:n.3565+147_3565+148insAGTC
XM_017009973.1:c.3544+147_3544+148insAGTC	XP_016865462.1:n.3544+147_3544+148insAGTC
XM_017009974.2:c.10447+147_10447+148insAGTC	XP_016865463.1:n.10447+147_10447+148insAGTC
XR_001742802.1:n.2522+11826_2522+11827insGACT
NR_003149.2:n.10442+147_10442+148insAGTC