Canonical Allele Identifier: CA2674568418

Gene: ADGRV1

Linked Data

• gnomAD v4: 5-90729072-TGTCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.90729074_90729077del , CM000667.2:g.90729074_90729077del	GRCh38
NC_000005.9:g.90024891_90024894del , CM000667.1:g.90024891_90024894del	GRCh37
NC_000005.8:g.90060647_90060650del	NCBI36
NG_007083.1:g.175275_175278del
NG_007083.2:g.204731_204734del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405460.9:c.10426+141_10426+144del MANE Select	ENSP00000384582.2:n.10426+141_10426+144del
ENST00000639431.1:c.265+52865_265+52868del	ENSP00000491057.1:n.265+52865_265+52868del
ENST00000640374.1:n.3570+141_3570+144del
ENST00000640464.1:n.845+141_845+144del
ENST00000405460.6:c.10426+141_10426+144del	ENSP00000384582.2:n.10426+141_10426+144del
ENST00000509621.1:c.3123+141_3123+144del
NM_032119.3:c.10426+141_10426+144del	NP_115495.3:n.10426+141_10426+144del
NR_003149.1:n.10439+141_10439+144del
XM_011543675.1:c.10423+141_10423+144del	XP_011541977.1:n.10423+141_10423+144del
XM_011543676.1:c.10345+141_10345+144del	XP_011541978.1:n.10345+141_10345+144del
XM_011543677.1:c.7729+141_7729+144del	XP_011541979.1:n.7729+141_7729+144del
XM_011543678.1:c.10426+141_10426+144del	XP_011541980.1:n.10426+141_10426+144del
XM_011543679.1:c.10426+141_10426+144del	XP_011541981.1:n.10426+141_10426+144del
XR_948560.1:n.271+11831_271+11834del
NM_032119.4:c.10426+141_10426+144del MANE Select	NP_115495.3:n.10426+141_10426+144del
XM_017009963.2:c.10447+141_10447+144del	XP_016865452.1:n.10447+141_10447+144del
XM_017009964.2:c.10444+141_10444+144del	XP_016865453.1:n.10444+141_10444+144del
XM_017009965.1:c.10444+141_10444+144del	XP_016865454.1:n.10444+141_10444+144del
XM_017009966.2:c.10366+141_10366+144del	XP_016865455.1:n.10366+141_10366+144del
XM_017009967.1:c.10351+141_10351+144del	XP_016865456.1:n.10351+141_10351+144del
XM_017009968.2:c.10447+141_10447+144del	XP_016865457.1:n.10447+141_10447+144del
XM_017009969.2:c.10447+141_10447+144del	XP_016865458.1:n.10447+141_10447+144del
XM_017009970.2:c.10447+141_10447+144del	XP_016865459.1:n.10447+141_10447+144del
XM_017009971.2:c.10447+141_10447+144del	XP_016865460.1:n.10447+141_10447+144del
XM_017009972.1:c.3565+141_3565+144del	XP_016865461.1:n.3565+141_3565+144del
XM_017009973.1:c.3544+141_3544+144del	XP_016865462.1:n.3544+141_3544+144del
XM_017009974.2:c.10447+141_10447+144del	XP_016865463.1:n.10447+141_10447+144del
XR_001742802.1:n.2522+11831_2522+11834del
NR_003149.2:n.10442+141_10442+144del